BEST1 Chromosome 11

Bestrophin 1
274 variants 274 Health Risk

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What This Gene Does
This gene encodes a member of the bestrophin gene family. This small gene family is characterized by proteins with a highly conserved N-terminus with four to six transmembrane domains. Bestrophins may form chloride ion channels or may regulate voltage-gated L-type calcium-ion channels. Bestrophins are generally believed to form calcium-activated chloride-ion channels in epithelial cells but they have also been shown to be highly permeable to bicarbonate ion transport in retinal tissue. Mutations in this gene are responsible for juvenile-onset vitelliform macular dystrophy (VMD2), also known as Best macular dystrophy, in addition to adult-onset vitelliform macular dystrophy (AVMD) and other retinopathies. Alternative splicing results in multiple variants encoding distinct isoforms.[provided by RefSeq, Nov 2008]
Gene Info
Gene Group
Bestrophins
Locus Type
gene with protein product
Location
11q12.3
Ensembl
ENSG00000167995
Associated Conditions (27)
Retinitis pigmentosa
BEST1-related disorder
Retinal dystrophy
Vitelliform macular dystrophy 2
Autosomal dominant vitreoretinochoroidopathy
Autosomal recessive bestrophinopathy
BEST1-related dominant retinopathy
Familial cancer of breast
Uterine carcinosarcoma
Thyroid cancer
nonmedullary
1
Malignant tumor of esophagus
Lung cancer
Retinitis pigmentosa 50
Inborn genetic diseases
Microcornea
rod-cone dystrophy
cataract
and posterior staphyloma 2
+7 more conditions
Key Variants
All Variants (274)
RSID Category Clinical Significance Conditions
RS1064796849 Health Risk Conflicting classifications of pathogenicity
RS112199774 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, BEST1-related disorder, Retinitis pigmentosa
RS1190983296 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Retinal dystrophy
RS1249897117 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Retinal dystrophy
RS138932379 Health Risk Conflicting classifications of pathogenicity
RS141071579 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, BEST1-related disorder, Retinitis pigmentosa
RS142482048 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinitis pigmentosa
RS144231113 Health Risk Conflicting classifications of pathogenicity Vitelliform macular dystrophy 2, Retinitis pigmentosa, Autosomal dominant vitreoretinochoroidopathy
RS145209035 Health Risk Conflicting classifications of pathogenicity BEST1-related disorder, BEST1-related disorder
RS147192139 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, BEST1-related disorder, Retinitis pigmentosa
RS147409760 Health Risk Conflicting classifications of pathogenicity Autosomal dominant vitreoretinochoroidopathy, Retinitis pigmentosa, Vitelliform macular dystrophy 2
RS150247275 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, BEST1-related disorder, Retinal dystrophy
RS1554963305 Health Risk Conflicting classifications of pathogenicity Autosomal recessive bestrophinopathy, Retinal dystrophy, Autosomal recessive bestrophinopathy
RS1555099968 Health Risk Conflicting classifications of pathogenicity Vitelliform macular dystrophy 2, Retinal dystrophy, Vitelliform macular dystrophy 2
RS17854138 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Retinal dystrophy, Retinitis pigmentosa
RS1805142 Health Risk Conflicting classifications of pathogenicity Vitelliform macular dystrophy 2, Retinal dystrophy, Vitelliform macular dystrophy 2
RS182941675 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Vitelliform macular dystrophy 2, Autosomal dominant vitreoretinochoroidopathy
RS1942209287 Health Risk Conflicting classifications of pathogenicity Autosomal recessive bestrophinopathy, Autosomal recessive bestrophinopathy
RS199998058 Health Risk Conflicting classifications of pathogenicity
RS201010315 Health Risk Conflicting classifications of pathogenicity Vitelliform macular dystrophy 2, Retinitis pigmentosa, Autosomal dominant vitreoretinochoroidopathy
RS201210799 Health Risk Conflicting classifications of pathogenicity
RS201386186 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, BEST1-related disorder, Retinal dystrophy
RS201586629 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Vitelliform macular dystrophy 2, Autosomal dominant vitreoretinochoroidopathy
RS2541372399 Health Risk Conflicting classifications of pathogenicity
RS2541377668 Health Risk Conflicting classifications of pathogenicity Autosomal recessive bestrophinopathy, Autosomal recessive bestrophinopathy
RS267606678 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa 50, Retinal dystrophy, Autosomal recessive bestrophinopathy
RS281865229 Health Risk Conflicting classifications of pathogenicity
RS281865532 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Retinal dystrophy
RS368387447 Health Risk Conflicting classifications of pathogenicity Vitelliform macular dystrophy 2, BEST1-related disorder, Vitelliform macular dystrophy 2
RS370397270 Health Risk Conflicting classifications of pathogenicity Vitelliform macular dystrophy 2, Retinitis pigmentosa, Autosomal dominant vitreoretinochoroidopathy
RS374772670 Health Risk Conflicting classifications of pathogenicity BEST1-related disorder, Inborn genetic diseases, BEST1-related disorder
RS375618932 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, BEST1-related disorder, Retinal dystrophy
RS563488311 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, BEST1-related disorder, Retinal dystrophy
RS62639356 Health Risk Conflicting classifications of pathogenicity Vitelliform macular dystrophy 2, Autosomal dominant vitreoretinochoroidopathy, Retinitis pigmentosa
RS748684128 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Retinal dystrophy
RS752923595 Health Risk Conflicting classifications of pathogenicity Autosomal dominant vitreoretinochoroidopathy, Retinal dystrophy, Vitelliform macular dystrophy 2
RS757536535 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Autosomal dominant vitreoretinochoroidopathy, Vitelliform macular dystrophy 2
RS759678509 Health Risk Conflicting classifications of pathogenicity Vitelliform macular dystrophy 2, Autosomal dominant vitreoretinochoroidopathy, Retinitis pigmentosa
RS760816505 Health Risk Conflicting classifications of pathogenicity Autosomal dominant vitreoretinochoroidopathy, Retinitis pigmentosa, Vitelliform macular dystrophy 2
RS764420497 Health Risk Conflicting classifications of pathogenicity Vitelliform macular dystrophy 2, Autosomal dominant vitreoretinochoroidopathy, Retinitis pigmentosa
RS765385264 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Autosomal recessive bestrophinopathy, BEST1-related dominant retinopathy
RS767436221 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS867577834 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS994248373 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Retinal dystrophy
RS1064793051 Health Risk Likely pathogenic
RS121918290 Health Risk Likely pathogenic Microcornea, rod-cone dystrophy, cataract
RS1299071387 Health Risk Likely pathogenic
RS1301396112 Health Risk Likely pathogenic
RS1334381137 Health Risk Likely pathogenic Autosomal recessive bestrophinopathy, Autosomal recessive bestrophinopathy
RS1382219910 Health Risk Likely pathogenic Retinal dystrophy, Retinal dystrophy
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