MAGEL2 Chromosome 15

MAGE family member L2
158 variants 158 Health Risk

Upload your DNA to see your personal genotypes for variants in MAGEL2.

What This Gene Does
Prader-Willi syndrome (PWS) is caused by the loss of expression of imprinted genes in chromosome 15q11-q13 region. Affected individuals exhibit neonatal hypotonia, developmental delay, and childhood-onset obesity. Necdin (NDN), a gene involved in the terminal differentiation of neurons, localizes to this region of the genome and has been implicated as one of the genes responsible for the etiology of PWS. This gene is structurally similar to NDN, is also localized to the PWS chromosomal region, and is paternally imprinted, suggesting a possible role for it in PWS. [provided by RefSeq, Oct 2010]
Gene Info
Gene Group
MAGE family
Locus Type
gene with protein product
Location
15q11.2
Ensembl
ENSG00000254585
Associated Conditions (14)
Inborn genetic diseases
MAGEL2-related disorder
Schaaf-Yang syndrome
Prader-Willi syndrome
Developmental disorder
Neurodevelopmental delay
See cases
Neurodevelopmental disorder
Prader-Willi-like syndrome
Ventriculomegaly
Multiple joint contractures
Generalized hypotonia
Ambiguous genitalia
Intellectual disability
Key Variants
All Variants (158)
RSID Category Clinical Significance Conditions
RS1033251181 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, MAGEL2-related disorder, Inborn genetic diseases
RS1045111596 Health Risk Conflicting classifications of pathogenicity MAGEL2-related disorder, Inborn genetic diseases, MAGEL2-related disorder
RS1176104366 Health Risk Conflicting classifications of pathogenicity Schaaf-Yang syndrome, Schaaf-Yang syndrome
RS1185550236 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, MAGEL2-related disorder, Inborn genetic diseases
RS1222522082 Health Risk Conflicting classifications of pathogenicity
RS1227406471 Health Risk Conflicting classifications of pathogenicity
RS1249139977 Health Risk Conflicting classifications of pathogenicity Schaaf-Yang syndrome, Schaaf-Yang syndrome
RS1386125417 Health Risk Conflicting classifications of pathogenicity
RS1433820460 Health Risk Conflicting classifications of pathogenicity
RS146970674 Health Risk Conflicting classifications of pathogenicity
RS1595331427 Health Risk Conflicting classifications of pathogenicity Schaaf-Yang syndrome, Schaaf-Yang syndrome
RS188762916 Health Risk Conflicting classifications of pathogenicity Prader-Willi syndrome, Inborn genetic diseases, Prader-Willi syndrome
RS1890404007 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, MAGEL2-related disorder, Inborn genetic diseases
RS199772480 Health Risk Conflicting classifications of pathogenicity Schaaf-Yang syndrome, Inborn genetic diseases, Schaaf-Yang syndrome
RS200478034 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS200958282 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS201811165 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, MAGEL2-related disorder, Inborn genetic diseases
RS201935129 Health Risk Conflicting classifications of pathogenicity Prader-Willi syndrome, Schaaf-Yang syndrome, Inborn genetic diseases
RS2233061 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS2503976271 Health Risk Conflicting classifications of pathogenicity
RS2503979002 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Schaaf-Yang syndrome, Inborn genetic diseases
RS34875116 Health Risk Conflicting classifications of pathogenicity
RS368008966 Health Risk Conflicting classifications of pathogenicity MAGEL2-related disorder, Inborn genetic diseases, MAGEL2-related disorder
RS368034669 Health Risk Conflicting classifications of pathogenicity MAGEL2-related disorder, MAGEL2-related disorder
RS368965952 Health Risk Conflicting classifications of pathogenicity Schaaf-Yang syndrome, Schaaf-Yang syndrome
RS369857789 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, MAGEL2-related disorder, Inborn genetic diseases
RS371119917 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS371613799 Health Risk Conflicting classifications of pathogenicity MAGEL2-related disorder, Inborn genetic diseases, MAGEL2-related disorder
RS372275206 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, MAGEL2-related disorder, Inborn genetic diseases
RS372352945 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS373183462 Health Risk Conflicting classifications of pathogenicity MAGEL2-related disorder, Inborn genetic diseases, MAGEL2-related disorder
RS373819727 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Schaaf-Yang syndrome, MAGEL2-related disorder
RS373945272 Health Risk Conflicting classifications of pathogenicity MAGEL2-related disorder, Inborn genetic diseases, MAGEL2-related disorder
RS528108868 Health Risk Conflicting classifications of pathogenicity
RS531503349 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, MAGEL2-related disorder, Inborn genetic diseases
RS541262134 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, MAGEL2-related disorder, Inborn genetic diseases
RS541606785 Health Risk Conflicting classifications of pathogenicity Prader-Willi syndrome, Schaaf-Yang syndrome, Inborn genetic diseases
RS543247133 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS544938560 Health Risk Conflicting classifications of pathogenicity
RS548982518 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS552582918 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Schaaf-Yang syndrome, Inborn genetic diseases
RS555920534 Health Risk Conflicting classifications of pathogenicity
RS556296973 Health Risk Conflicting classifications of pathogenicity MAGEL2-related disorder, Inborn genetic diseases, MAGEL2-related disorder
RS558186319 Health Risk Conflicting classifications of pathogenicity MAGEL2-related disorder, MAGEL2-related disorder
RS570335069 Health Risk Conflicting classifications of pathogenicity
RS572249702 Health Risk Conflicting classifications of pathogenicity Schaaf-Yang syndrome, Inborn genetic diseases, Schaaf-Yang syndrome
RS576073679 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, MAGEL2-related disorder, Inborn genetic diseases
RS58729661 Health Risk Conflicting classifications of pathogenicity Schaaf-Yang syndrome, Inborn genetic diseases, Schaaf-Yang syndrome
RS745776063 Health Risk Conflicting classifications of pathogenicity MAGEL2-related disorder, MAGEL2-related disorder
RS749726173 Health Risk Conflicting classifications of pathogenicity MAGEL2-related disorder, Inborn genetic diseases, MAGEL2-related disorder
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