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rs876657674

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876657674(-;-)
Make rs876657674(-;G)
Make rs876657674(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position74074790
GeneVCL
is asnp
is mentioned by
dbSNPrs876657674
ebirs876657674
HLIrs876657674
Exacrs876657674
Varsomers876657674
Maprs876657674
PheGenIrs876657674
hapmaprs876657674
1000 genomesrs876657674
hgdprs876657674
ensemblrs876657674
gopubmedrs876657674
geneviewrs876657674
scholarrs876657674
googlers876657674
pharmgkbrs876657674
gwascentralrs876657674
openSNPrs876657674
23andMers876657674
23andMe allrs876657674
SNP Nexus

SNPshotrs876657674
SNPdbers876657674
MSV3drs876657674
GWAS Ctlgrs876657674
Max Magnitude0
ClinVar
Risk rs876657674(G;G)
Alt rs876657674(G;G)
Reference rs876657674(;)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene VCL
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000010.10:g.75834548dupG
CLNSRC
CLNACC RCV000221392.1,