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rs876657662

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657662(A;A)
Make rs876657662(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position63060872
GeneTPM1
is asnp
is mentioned by
dbSNPrs876657662
ebirs876657662
HLIrs876657662
Exacrs876657662
Varsomers876657662
Maprs876657662
PheGenIrs876657662
hapmaprs876657662
1000 genomesrs876657662
hgdprs876657662
ensemblrs876657662
gopubmedrs876657662
geneviewrs876657662
scholarrs876657662
googlers876657662
pharmgkbrs876657662
gwascentralrs876657662
openSNPrs876657662
23andMers876657662
23andMe allrs876657662
SNP Nexus

SNPshotrs876657662
SNPdbers876657662
MSV3drs876657662
GWAS Ctlgrs876657662
Max Magnitude0
ClinVar
Risk rs876657662(A;A)
Alt rs876657662(A;A)
Reference rs876657662(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TPM1
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000015.9:g.63353071G>A
CLNSRC
CLNACC RCV000221536.1,