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rs121909377

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909377(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position47333238
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs121909377
ebirs121909377
HLIrs121909377
Exacrs121909377
Varsomers121909377
Maprs121909377
PheGenIrs121909377
hapmaprs121909377
1000 genomesrs121909377
hgdprs121909377
ensemblrs121909377
gopubmedrs121909377
geneviewrs121909377
scholarrs121909377
googlers121909377
pharmgkbrs121909377
gwascentralrs121909377
openSNPrs121909377
23andMers121909377
23andMe allrs121909377
SNP Nexus

SNPshotrs121909377
SNPdbers121909377
MSV3drs121909377
GWAS Ctlgrs121909377
Max Magnitude0
OMIM600958
Desc
Variant0014
Relatedalso
ClinVar
Risk rs121909377(A,T;A,T)
Alt rs121909377(A,T;A,T)
Reference rs121909377(G;G)
Significance Other
Disease Familial hypertrophic cardiomyopathy 4 not provided Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Familial hypertrophic cardiomyopathy 4 not provided Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000011.9:g.47354789C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009147.5, RCV000158223.2, RCV000211819.1,