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rs397517244

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397517244(C;T)
Make rs397517244(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position74072792
GeneVCL
is asnp
is mentioned by
dbSNPrs397517244
ebirs397517244
HLIrs397517244
Exacrs397517244
Varsomers397517244
Maprs397517244
PheGenIrs397517244
hapmaprs397517244
1000 genomesrs397517244
hgdprs397517244
ensemblrs397517244
gopubmedrs397517244
geneviewrs397517244
scholarrs397517244
googlers397517244
pharmgkbrs397517244
gwascentralrs397517244
openSNPrs397517244
23andMers397517244
23andMe allrs397517244
SNP Nexus

SNPshotrs397517244
SNPdbers397517244
MSV3drs397517244
GWAS Ctlgrs397517244
Max Magnitude0
ClinVar
Risk rs397517244(T;T)
Alt rs397517244(T;T)
Reference rs397517244(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy not specified
Variation info
Gene VCL
CLNDBN Primary dilated cardiomyopathy not specified
Reversed 0
HGVS NC_000010.10:g.75832550C>T
CLNSRC ClinVar
CLNACC RCV000038833.2, RCV000183988.2,