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rs121913631

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913631(C;G)
Make rs121913631(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23424107
GeneMYH7
is asnp
is mentioned by
dbSNPrs121913631
ebirs121913631
HLIrs121913631
Exacrs121913631
Varsomers121913631
Maprs121913631
PheGenIrs121913631
hapmaprs121913631
1000 genomesrs121913631
hgdprs121913631
ensemblrs121913631
gopubmedrs121913631
geneviewrs121913631
scholarrs121913631
googlers121913631
pharmgkbrs121913631
gwascentralrs121913631
openSNPrs121913631
23andMers121913631
23andMe allrs121913631
SNP Nexus

SNPshotrs121913631
SNPdbers121913631
MSV3drs121913631
GWAS Ctlgrs121913631
Max Magnitude0
OMIM160760
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121913631(G;G)
Alt rs121913631(G;G)
Reference rs121913631(C;C)
Significance Other
Disease Familial hypertrophic cardiomyopathy 1 Primary familial hypertrophic cardiomyopathy not provided
Variation info
Gene MYH7
CLNDBN Familial hypertrophic cardiomyopathy 1 Primary familial hypertrophic cardiomyopathy not provided
Reversed 1
HGVS NC_000014.8:g.23893316G>C
CLNSRC HGMD OMIM Allelic Variant
CLNACC RCV000015153.27, RCV000035820.3, RCV000078452.5,