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rs367947846

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs367947846(A;A)
Make rs367947846(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47346298
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs367947846
ebirs367947846
HLIrs367947846
Exacrs367947846
Varsomers367947846
Maprs367947846
PheGenIrs367947846
hapmaprs367947846
1000 genomesrs367947846
hgdprs367947846
ensemblrs367947846
gopubmedrs367947846
geneviewrs367947846
scholarrs367947846
googlers367947846
pharmgkbrs367947846
gwascentralrs367947846
openSNPrs367947846
23andMers367947846
23andMe allrs367947846
SNP Nexus

SNPshotrs367947846
SNPdbers367947846
MSV3drs367947846
GWAS Ctlgrs367947846
Max Magnitude0
ClinVar
Risk rs367947846(A,C;A,C)
Alt rs367947846(A,C;A,C)
Reference rs367947846(G;G)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 0
HGVS NC_000011.9:g.47367849G>C
CLNSRC
CLNACC RCV000154309.2,