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rs876657634

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876657634(C;T)
Make rs876657634(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position119672477
GeneBAG3
is asnp
is mentioned by
dbSNPrs876657634
ebirs876657634
HLIrs876657634
Exacrs876657634
Varsomers876657634
Maprs876657634
PheGenIrs876657634
hapmaprs876657634
1000 genomesrs876657634
hgdprs876657634
ensemblrs876657634
gopubmedrs876657634
geneviewrs876657634
scholarrs876657634
googlers876657634
pharmgkbrs876657634
gwascentralrs876657634
openSNPrs876657634
23andMers876657634
23andMe allrs876657634
SNP Nexus

SNPshotrs876657634
SNPdbers876657634
MSV3drs876657634
GWAS Ctlgrs876657634
Max Magnitude0
ClinVar
Risk rs876657634(T;T)
Alt rs876657634(T;T)
Reference rs876657634(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene BAG3
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000010.10:g.121431989C>T
CLNSRC
CLNACC RCV000215570.1,