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rs397517406

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397517406(C;G)
Make rs397517406(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position31086672
GeneDSC2
is asnp
is mentioned by
dbSNPrs397517406
ebirs397517406
HLIrs397517406
Exacrs397517406
Varsomers397517406
Maprs397517406
PheGenIrs397517406
hapmaprs397517406
1000 genomesrs397517406
hgdprs397517406
ensemblrs397517406
gopubmedrs397517406
geneviewrs397517406
scholarrs397517406
googlers397517406
pharmgkbrs397517406
gwascentralrs397517406
openSNPrs397517406
23andMers397517406
23andMe allrs397517406
SNP Nexus

SNPshotrs397517406
SNPdbers397517406
MSV3drs397517406
GWAS Ctlgrs397517406
Max Magnitude0
ClinVar
Risk rs397517406(G;G)
Alt rs397517406(G;G)
Reference rs397517406(C;C)
Significance Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy not provided
Variation info
Gene DSC2
CLNDBN Arrhythmogenic right ventricular cardiomyopathy not provided
Reversed 1
HGVS NC_000018.9:g.28666635G>C
CLNSRC ClinVar
CLNACC RCV000039442.2, RCV000181144.2,