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rs121913007

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913007(A;A)
Make rs121913007(A;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position31524792
GeneDSG2
is asnp
is mentioned by
dbSNPrs121913007
ebirs121913007
HLIrs121913007
Exacrs121913007
Varsomers121913007
Maprs121913007
PheGenIrs121913007
hapmaprs121913007
1000 genomesrs121913007
hgdprs121913007
ensemblrs121913007
gopubmedrs121913007
geneviewrs121913007
scholarrs121913007
googlers121913007
pharmgkbrs121913007
gwascentralrs121913007
openSNPrs121913007
23andMers121913007
23andMe allrs121913007
SNP Nexus

SNPshotrs121913007
SNPdbers121913007
MSV3drs121913007
GWAS Ctlgrs121913007
Max Magnitude0
OMIM125671
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121913007(A;A)
Alt rs121913007(A;A)
Reference rs121913007(G;G)
Significance Pathogenic
Disease Arrhythmogenic right ventricular cardiomyopathy not provided
Variation info
Gene DSG2
CLNDBN Arrhythmogenic right ventricular cardiomyopathy, type 10 not provided
Reversed 0
HGVS NC_000018.9:g.29104755G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018304.30, RCV000181248.1,