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rs397517239

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397517239(C;T)
Make rs397517239(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position74070743
GeneVCL
is asnp
is mentioned by
dbSNPrs397517239
ebirs397517239
HLIrs397517239
Exacrs397517239
Varsomers397517239
Maprs397517239
PheGenIrs397517239
hapmaprs397517239
1000 genomesrs397517239
hgdprs397517239
ensemblrs397517239
gopubmedrs397517239
geneviewrs397517239
scholarrs397517239
googlers397517239
pharmgkbrs397517239
gwascentralrs397517239
openSNPrs397517239
23andMers397517239
23andMe allrs397517239
SNP Nexus

SNPshotrs397517239
SNPdbers397517239
MSV3drs397517239
GWAS Ctlgrs397517239
Max Magnitude0
ClinVar
Risk rs397517239(T;T)
Alt rs397517239(T;T)
Reference rs397517239(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene VCL
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000010.10:g.75830501C>T
CLNSRC ClinVar
CLNACC RCV000038823.2,