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rs373056282

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs373056282(A;A)
Make rs373056282(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position47335065
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs373056282
ebirs373056282
HLIrs373056282
Exacrs373056282
Varsomers373056282
Maprs373056282
PheGenIrs373056282
hapmaprs373056282
1000 genomesrs373056282
hgdprs373056282
ensemblrs373056282
gopubmedrs373056282
geneviewrs373056282
scholarrs373056282
googlers373056282
pharmgkbrs373056282
gwascentralrs373056282
openSNPrs373056282
23andMers373056282
23andMe allrs373056282
SNP Nexus

SNPshotrs373056282
SNPdbers373056282
MSV3drs373056282
GWAS Ctlgrs373056282
Max Magnitude0
ClinVar
Risk rs373056282(A;A)
Alt rs373056282(A;A)
Reference rs373056282(G;G)
Significance Pathogenic
Disease not specified Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN not specified Primary familial hypertrophic cardiomyopathy
Reversed 0
HGVS NC_000011.9:g.47356616G>A
CLNSRC ClinVar OMIM Allelic Variant University of Washington
CLNACC RCV000035536.5, RCV000148673.1,