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rs564378953

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs564378953(C;T)
Make rs564378953(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47338649
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs564378953
ebirs564378953
HLIrs564378953
Exacrs564378953
Varsomers564378953
Maprs564378953
PheGenIrs564378953
hapmaprs564378953
1000 genomesrs564378953
hgdprs564378953
ensemblrs564378953
gopubmedrs564378953
geneviewrs564378953
scholarrs564378953
googlers564378953
pharmgkbrs564378953
gwascentralrs564378953
openSNPrs564378953
23andMers564378953
23andMe allrs564378953
SNP Nexus

SNPshotrs564378953
SNPdbers564378953
MSV3drs564378953
GWAS Ctlgrs564378953
Max Magnitude0
ClinVar
Risk rs564378953(T;T)
Alt rs564378953(T;T)
Reference rs564378953(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.47360200C>T
CLNSRC
CLNACC RCV000158140.2,