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rs794728098

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs794728098(-;-)
Make rs794728098(-;CA)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position31545758
GeneDSG2, DSG2-AS1
is asnp
is mentioned by
dbSNPrs794728098
ClinGenrs794728098
ebirs794728098
HLIrs794728098
Exacrs794728098
Varsomers794728098
Maprs794728098
PheGenIrs794728098
hapmaprs794728098
1000 genomesrs794728098
hgdprs794728098
ensemblrs794728098
gopubmedrs794728098
geneviewrs794728098
scholarrs794728098
googlers794728098
pharmgkbrs794728098
gwascentralrs794728098
openSNPrs794728098
23andMers794728098
23andMe allrs794728098
SNP Nexus

SNPshotrs794728098
SNPdbers794728098
MSV3drs794728098
GWAS Ctlgrs794728098
Max Magnitude0
ClinVar
Risk rs794728098(-;-)
Alt rs794728098(-;-)
Reference Rs794728098(CA;CA)
Significance Pathogenic
Disease not provided
Variation info
Gene DSG2-AS1 DSG2
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.29125721_29125722delCA
CLNSRC
CLNACC RCV000181250.1,