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rs121913008

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913008(A;A)
Make rs121913008(A;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position31519858
GeneDSG2
is asnp
is mentioned by
dbSNPrs121913008
ebirs121913008
HLIrs121913008
Exacrs121913008
Varsomers121913008
Maprs121913008
PheGenIrs121913008
hapmaprs121913008
1000 genomesrs121913008
hgdprs121913008
ensemblrs121913008
gopubmedrs121913008
geneviewrs121913008
scholarrs121913008
googlers121913008
pharmgkbrs121913008
gwascentralrs121913008
openSNPrs121913008
23andMers121913008
23andMe allrs121913008
SNP Nexus

SNPshotrs121913008
SNPdbers121913008
MSV3drs121913008
GWAS Ctlgrs121913008
Max Magnitude0
OMIM125671
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121913008(A;A)
Alt rs121913008(A;A)
Reference rs121913008(G;G)
Significance Other
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.29099821G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018305.32, RCV000181197.2, RCV000211714.1,