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rs372371774

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs372371774(C;C)
Make rs372371774(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47341221
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs372371774
ebirs372371774
HLIrs372371774
Exacrs372371774
Varsomers372371774
Maprs372371774
PheGenIrs372371774
hapmaprs372371774
1000 genomesrs372371774
hgdprs372371774
ensemblrs372371774
gopubmedrs372371774
geneviewrs372371774
scholarrs372371774
googlers372371774
pharmgkbrs372371774
gwascentralrs372371774
openSNPrs372371774
23andMers372371774
23andMe allrs372371774
SNP Nexus

SNPshotrs372371774
SNPdbers372371774
MSV3drs372371774
GWAS Ctlgrs372371774
Max Magnitude0
ClinVar
Risk rs372371774(C;C)
Alt rs372371774(C;C)
Reference rs372371774(T;T)
Significance Pathogenic
Disease not specified Primary dilated cardiomyopathy
Variation info
Gene MYBPC3
CLNDBN not specified Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000011.9:g.47362772T>C
CLNSRC
CLNACC RCV000035440.2, RCV000157309.1,