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rs397517395

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397517395(G;G)
Make rs397517395(G;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position31071792
GeneDSC2
is asnp
is mentioned by
dbSNPrs397517395
ebirs397517395
HLIrs397517395
Exacrs397517395
Varsomers397517395
Maprs397517395
PheGenIrs397517395
hapmaprs397517395
1000 genomesrs397517395
hgdprs397517395
ensemblrs397517395
gopubmedrs397517395
geneviewrs397517395
scholarrs397517395
googlers397517395
pharmgkbrs397517395
gwascentralrs397517395
openSNPrs397517395
23andMers397517395
23andMe allrs397517395
SNP Nexus

SNPshotrs397517395
SNPdbers397517395
MSV3drs397517395
GWAS Ctlgrs397517395
Max Magnitude0
ClinVar
Risk rs397517395(G;G)
Alt rs397517395(G;G)
Reference rs397517395(T;T)
Significance Probable-Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene DSC2
CLNDBN Arrhythmogenic right ventricular cardiomyopathy
Reversed 1
HGVS NC_000018.9:g.28651758A>C
CLNSRC ClinVar
CLNACC RCV000039415.2,