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rs150516929

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs150516929(C;T)
Make rs150516929(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position111908832
GeneCRYAB
is asnp
is mentioned by
dbSNPrs150516929
ebirs150516929
HLIrs150516929
Exacrs150516929
Varsomers150516929
Maprs150516929
PheGenIrs150516929
hapmaprs150516929
1000 genomesrs150516929
hgdprs150516929
ensemblrs150516929
gopubmedrs150516929
geneviewrs150516929
scholarrs150516929
googlers150516929
pharmgkbrs150516929
gwascentralrs150516929
openSNPrs150516929
23andMers150516929
23andMe allrs150516929
SNP Nexus

SNPshotrs150516929
SNPdbers150516929
MSV3drs150516929
GWAS Ctlgrs150516929
Max Magnitude0
ClinVar
Risk rs150516929(T;T)
Alt rs150516929(T;T)
Reference rs150516929(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 1II not specified Primary familial hypertrophic cardiomyopathy not provided Congenital cataract
Variation info
Gene CRYAB
CLNDBN Dilated cardiomyopathy 1II not specified Primary familial hypertrophic cardiomyopathy not provided Congenital cataract
Reversed 0
HGVS NC_000011.9:g.111779556C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000034839.24, RCV000037217.3, RCV000157153.1, RCV000177141.3, RCV000203359.1,