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rs587776700

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587776700(C;G)
Make rs587776700(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position47347030
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs587776700
ebirs587776700
HLIrs587776700
Exacrs587776700
Varsomers587776700
Maprs587776700
PheGenIrs587776700
hapmaprs587776700
1000 genomesrs587776700
hgdprs587776700
ensemblrs587776700
gopubmedrs587776700
geneviewrs587776700
scholarrs587776700
googlers587776700
pharmgkbrs587776700
gwascentralrs587776700
openSNPrs587776700
23andMers587776700
23andMe allrs587776700
SNP Nexus

SNPshotrs587776700
SNPdbers587776700
MSV3drs587776700
GWAS Ctlgrs587776700
Max Magnitude0
ClinVar
Risk rs587776700(G;G)
Alt rs587776700(G;G)
Reference rs587776700(C;C)
Significance Pathogenic
Disease Familial hypertrophic cardiomyopathy 4 not provided
Variation info
Gene MYBPC3
CLNDBN Familial hypertrophic cardiomyopathy 4 not provided
Reversed 0
HGVS NC_000011.9:g.47368581C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000009150.4, RCV000158319.2,