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rs397517389

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397517389(G;G)
Make rs397517389(G;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position31082924
GeneDSC2
is asnp
is mentioned by
dbSNPrs397517389
ebirs397517389
HLIrs397517389
Exacrs397517389
Varsomers397517389
Maprs397517389
PheGenIrs397517389
hapmaprs397517389
1000 genomesrs397517389
hgdprs397517389
ensemblrs397517389
gopubmedrs397517389
geneviewrs397517389
scholarrs397517389
googlers397517389
pharmgkbrs397517389
gwascentralrs397517389
openSNPrs397517389
23andMers397517389
23andMe allrs397517389
SNP Nexus

SNPshotrs397517389
SNPdbers397517389
MSV3drs397517389
GWAS Ctlgrs397517389
Max Magnitude0
ClinVar
Risk rs397517389(G;G)
Alt rs397517389(G;G)
Reference rs397517389(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.28662890A>C
CLNSRC ClinVar
CLNACC RCV000039401.2,