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rs397517245

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397517245(-;-)
Make rs397517245(-;A)
Make rs397517245(A;A)
ReferenceGRCh38 38.1/141
Chromosome10
Position74074779
GeneVCL
is asnp
is mentioned by
dbSNPrs397517245
ebirs397517245
HLIrs397517245
Exacrs397517245
Varsomers397517245
Maprs397517245
PheGenIrs397517245
hapmaprs397517245
1000 genomesrs397517245
hgdprs397517245
ensemblrs397517245
gopubmedrs397517245
geneviewrs397517245
scholarrs397517245
googlers397517245
pharmgkbrs397517245
gwascentralrs397517245
openSNPrs397517245
23andMers397517245
23andMe allrs397517245
SNP Nexus

SNPshotrs397517245
SNPdbers397517245
MSV3drs397517245
GWAS Ctlgrs397517245
Max Magnitude0
ClinVar
Risk rs397517245(A;A)
Alt rs397517245(A;A)
Reference rs397517245(;)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene VCL
CLNDBN Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000010.10:g.75834537dupA
CLNSRC ClinVar
CLNACC RCV000038836.2,