Have questions? Visit https://www.reddit.com/r/SNPedia

rs794728086

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728086(C;T)
Make rs794728086(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position31538849
GeneDSG2
is asnp
is mentioned by
dbSNPrs794728086
ebirs794728086
HLIrs794728086
Exacrs794728086
Varsomers794728086
Maprs794728086
PheGenIrs794728086
hapmaprs794728086
1000 genomesrs794728086
hgdprs794728086
ensemblrs794728086
gopubmedrs794728086
geneviewrs794728086
scholarrs794728086
googlers794728086
pharmgkbrs794728086
gwascentralrs794728086
openSNPrs794728086
23andMers794728086
23andMe allrs794728086
SNP Nexus

SNPshotrs794728086
SNPdbers794728086
MSV3drs794728086
GWAS Ctlgrs794728086
Max Magnitude0
ClinVar
Risk rs794728086(T;T)
Alt rs794728086(T;T)
Reference rs794728086(C;C)
Significance Pathogenic
Disease not provided Arrhythmogenic right ventricular cardiomyopathy
Variation info
Gene DSG2
CLNDBN not provided Arrhythmogenic right ventricular cardiomyopathy, type 10
Reversed 0
HGVS NC_000018.9:g.29118812C>T
CLNSRC
CLNACC RCV000181222.1, RCV000227785.1,