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rs397517234

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397517234(C;T)
Make rs397517234(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position74095751
GeneVCL
is asnp
is mentioned by
dbSNPrs397517234
ebirs397517234
HLIrs397517234
Exacrs397517234
Varsomers397517234
Maprs397517234
PheGenIrs397517234
hapmaprs397517234
1000 genomesrs397517234
hgdprs397517234
ensemblrs397517234
gopubmedrs397517234
geneviewrs397517234
scholarrs397517234
googlers397517234
pharmgkbrs397517234
gwascentralrs397517234
openSNPrs397517234
23andMers397517234
23andMe allrs397517234
SNP Nexus

SNPshotrs397517234
SNPdbers397517234
MSV3drs397517234
GWAS Ctlgrs397517234
Max Magnitude0
ClinVar
Risk rs397517234(T;T)
Alt rs397517234(T;T)
Reference rs397517234(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene VCL
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000010.10:g.75855509C>T
CLNSRC ClinVar
CLNACC RCV000038802.3,