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rs397514038

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397514038(A;G)
Make rs397514038(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position31541191
GeneDSG2
is asnp
is mentioned by
dbSNPrs397514038
ebirs397514038
HLIrs397514038
Exacrs397514038
Varsomers397514038
Maprs397514038
PheGenIrs397514038
hapmaprs397514038
1000 genomesrs397514038
hgdprs397514038
ensemblrs397514038
gopubmedrs397514038
geneviewrs397514038
scholarrs397514038
googlers397514038
pharmgkbrs397514038
gwascentralrs397514038
openSNPrs397514038
23andMers397514038
23andMe allrs397514038
SNP Nexus

SNPshotrs397514038
SNPdbers397514038
MSV3drs397514038
GWAS Ctlgrs397514038
Max Magnitude0
ClinVar
Risk rs397514038(G;G)
Alt rs397514038(G;G)
Reference rs397514038(A;A)
Significance Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy not provided Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene DSG2
CLNDBN Arrhythmogenic right ventricular cardiomyopathy, type 10 not provided Arrhythmogenic right ventricular cardiomyopathy
Reversed 0
HGVS NC_000018.9:g.29121154A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000018310.31, RCV000181225.1, RCV000211716.1,