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rs794728091

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs794728091(-;T)
Make rs794728091(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position31521184
GeneDSG2
is asnp
is mentioned by
dbSNPrs794728091
ClinGenrs794728091
ebirs794728091
HLIrs794728091
Exacrs794728091
Varsomers794728091
Maprs794728091
PheGenIrs794728091
hapmaprs794728091
1000 genomesrs794728091
hgdprs794728091
ensemblrs794728091
gopubmedrs794728091
geneviewrs794728091
scholarrs794728091
googlers794728091
pharmgkbrs794728091
gwascentralrs794728091
openSNPrs794728091
23andMers794728091
23andMe allrs794728091
SNP Nexus

SNPshotrs794728091
SNPdbers794728091
MSV3drs794728091
GWAS Ctlgrs794728091
Max Magnitude0
ClinVar
Risk rs794728091(T;T)
Alt rs794728091(T;T)
Reference Rs794728091(-;-)
Significance Pathogenic
Disease Cardiomyopathy
Variation info
Gene DSG2
CLNDBN Cardiomyopathy
Reversed 0
HGVS NC_000018.9:g.29101147_29101148insT
CLNSRC
CLNACC RCV000181238.1,