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rs121913632

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913632(C;C)
Make rs121913632(C;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23425760
GeneMYH7
is asnp
is mentioned by
dbSNPrs121913632
ebirs121913632
HLIrs121913632
Exacrs121913632
Varsomers121913632
Maprs121913632
PheGenIrs121913632
hapmaprs121913632
1000 genomesrs121913632
hgdprs121913632
ensemblrs121913632
gopubmedrs121913632
geneviewrs121913632
scholarrs121913632
googlers121913632
pharmgkbrs121913632
gwascentralrs121913632
openSNPrs121913632
23andMers121913632
23andMe allrs121913632
SNP Nexus

SNPshotrs121913632
SNPdbers121913632
MSV3drs121913632
GWAS Ctlgrs121913632
Max Magnitude0
OMIM160760
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121913632(A,C,T;A,C,T)
Alt rs121913632(A,C,T;A,C,T)
Reference rs121913632(G;G)
Significance Other
Disease Primary familial hypertrophic cardiomyopathy not provided Familial hypertrophic cardiomyopathy 1 not specified
Variation info
Gene MYH7
CLNDBN Primary familial hypertrophic cardiomyopathy not provided Familial hypertrophic cardiomyopathy 1 not specified
Reversed 1
HGVS NC_000014.8:g.23894969C>A; NC_000014.8:g.23894969C>G; NC_000014.8:g.23894969C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000154255.1, RCV000158523.2, RCV000162338.2, RCV000168866.1, RCV000015154.27, RCV000035779.3, RCV000158522.2, RCV000035778.3, RCV000158521.2, RCV000168865.1,