LAMA2 Chromosome 6

Laminin subunit alpha 2
1142 variants 1142 Health Risk

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What This Gene Does
Laminin, an extracellular protein, is a major component of the basement membrane. It is thought to mediate the attachment, migration, and organization of cells into tissues during embryonic development by interacting with other extracellular matrix components. It is composed of three subunits, alpha, beta, and gamma, which are bound to each other by disulfide bonds into a cross-shaped molecule. This gene encodes the alpha 2 chain, which constitutes one of the subunits of laminin 2 (merosin) and laminin 4 (s-merosin). Mutations in this gene have been identified as the cause of congenital merosin-deficient muscular dystrophy. Two transcript variants encoding different proteins have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Laminin subunits
Locus Type
gene with protein product
Location
6q22.33
Ensembl
ENSG00000196569
Associated Conditions (35)
Merosin deficient congenital muscular dystrophy
LAMA2-related muscular dystrophy
Myalgia
Elevated circulating creatine kinase concentration
Exercise-induced myalgia
Muscular dystrophy
limb-girdle
autosomal recessive 23
Congenital muscular dystrophy due to partial LAMA2 deficiency
LAMA2-related disorder
Intellectual disability
Inborn genetic diseases
Malignant tumor of esophagus
Primary dilated cardiomyopathy
Malignant tumor of urinary bladder
Familial cancer of breast
Ovarian cancer
Cervical cancer
Rare genetic intellectual disability
See cases
+15 more conditions
Key Variants
RS1012171328
Conflicting classifications of pathogenicity
Merosin deficient congenital muscular dystrophy, LAMA2-related muscular dystrophy, Merosin deficient congenital muscular dystrophy
Health Risk
RS1024374408
Conflicting classifications of pathogenicity
Myalgia, Elevated circulating creatine kinase concentration, Exercise-induced myalgia
Health Risk
RS1057523624
Conflicting classifications of pathogenicity
LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
Health Risk
RS1057524616
Conflicting classifications of pathogenicity
LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
Health Risk
RS1064795750
Conflicting classifications of pathogenicity
Muscular dystrophy, limb-girdle, autosomal recessive 23
Health Risk
RS111632017
Conflicting classifications of pathogenicity
Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related disorder, LAMA2-related muscular dystrophy
Health Risk
RS112388307
Conflicting classifications of pathogenicity
LAMA2-related muscular dystrophy, LAMA2-related disorder, LAMA2-related muscular dystrophy
Health Risk
RS112637707
Conflicting classifications of pathogenicity
LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related disorder
Health Risk
RS113022759
Conflicting classifications of pathogenicity
LAMA2-related muscular dystrophy, Merosin deficient congenital muscular dystrophy, Muscular dystrophy
Health Risk
RS115488979
Conflicting classifications of pathogenicity
Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy, LAMA2-related disorder
Health Risk
RS115650537
Conflicting classifications of pathogenicity
LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related disorder
Health Risk
RS117116822
Conflicting classifications of pathogenicity
LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related disorder
Health Risk
All Variants (1142)
RSID Category Clinical Significance Conditions
RS149347601 Health Risk Conflicting classifications of pathogenicity Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency
RS149487202 Health Risk Conflicting classifications of pathogenicity Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency
RS149753273 Health Risk Conflicting classifications of pathogenicity Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency
RS150046431 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS150237160 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Inborn genetic diseases, LAMA2-related muscular dystrophy
RS150394215 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency, Merosin deficient congenital muscular dystrophy
RS150596964 Health Risk Conflicting classifications of pathogenicity Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency
RS150644209 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, LAMA2-related disorder, Inborn genetic diseases
RS150691000 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS150730793 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS150945378 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, LAMA2-related disorder, LAMA2-related muscular dystrophy
RS151009169 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, LAMA2-related disorder, LAMA2-related muscular dystrophy
RS151049890 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Muscular dystrophy, limb-girdle
RS151334775 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS1554285766 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS1554310330 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Merosin deficient congenital muscular dystrophy, LAMA2-related muscular dystrophy
RS1562581016 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS1583133494 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Merosin deficient congenital muscular dystrophy, LAMA2-related muscular dystrophy
RS1776320682 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS1777983774 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS182958473 Health Risk Conflicting classifications of pathogenicity Congenital muscular dystrophy due to partial LAMA2 deficiency, Inborn genetic diseases, Muscular dystrophy
RS183890063 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, LAMA2-related muscular dystrophy, Inborn genetic diseases
RS184127828 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency, Merosin deficient congenital muscular dystrophy
RS188069926 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Inborn genetic diseases, LAMA2-related muscular dystrophy
RS189360899 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy
RS190362395 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Inborn genetic diseases, LAMA2-related muscular dystrophy
RS191215452 Health Risk Conflicting classifications of pathogenicity Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency
RS191899712 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Merosin deficient congenital muscular dystrophy, LAMA2-related muscular dystrophy
RS192650285 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy
RS199570699 Health Risk Conflicting classifications of pathogenicity Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency
RS199814707 Health Risk Conflicting classifications of pathogenicity Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy, Merosin deficient congenital muscular dystrophy
RS199904029 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy
RS199931560 Health Risk Conflicting classifications of pathogenicity Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency
RS200030296 Health Risk Conflicting classifications of pathogenicity Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy, LAMA2-related disorder
RS200123250 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Inborn genetic diseases, LAMA2-related muscular dystrophy
RS200224891 Health Risk Conflicting classifications of pathogenicity Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency
RS200341138 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency, Inborn genetic diseases
RS200364660 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS200469923 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related disorder
RS200518204 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy
RS200646230 Health Risk Conflicting classifications of pathogenicity Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency
RS200705442 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency, Inborn genetic diseases
RS200718262 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS200796753 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy
RS200928844 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS200953311 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related disorder
RS200961385 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS201041465 Health Risk Conflicting classifications of pathogenicity Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy, Congenital muscular dystrophy due to partial LAMA2 deficiency
RS201122410 Health Risk Conflicting classifications of pathogenicity LAMA2-related muscular dystrophy, LAMA2-related muscular dystrophy
RS201172088 Health Risk Conflicting classifications of pathogenicity Congenital muscular dystrophy due to partial LAMA2 deficiency, LAMA2-related muscular dystrophy, Inborn genetic diseases
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