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rs121913006

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913006(A;A)
Make rs121913006(A;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position31519867
GeneDSG2
is asnp
is mentioned by
dbSNPrs121913006
ebirs121913006
HLIrs121913006
Exacrs121913006
Varsomers121913006
Maprs121913006
PheGenIrs121913006
hapmaprs121913006
1000 genomesrs121913006
hgdprs121913006
ensemblrs121913006
gopubmedrs121913006
geneviewrs121913006
scholarrs121913006
googlers121913006
pharmgkbrs121913006
gwascentralrs121913006
openSNPrs121913006
23andMers121913006
23andMe allrs121913006
SNP Nexus

SNPshotrs121913006
SNPdbers121913006
MSV3drs121913006
GWAS Ctlgrs121913006
Max Magnitude0
OMIM125671
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121913006(A;A)
Alt rs121913006(A;A)
Reference rs121913006(G;G)
Significance Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy Cardiomyopathy Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene DSG2
CLNDBN Arrhythmogenic right ventricular cardiomyopathy, type 10 Cardiomyopathy Arrhythmogenic right ventricular cardiomyopathy
Reversed 0
HGVS NC_000018.9:g.29099830G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018303.28, RCV000181198.1, RCV000211715.1,