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rs794728090

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728090(C;G)
Make rs794728090(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position31545785
GeneDSG2, DSG2-AS1
is asnp
is mentioned by
dbSNPrs794728090
ebirs794728090
HLIrs794728090
Exacrs794728090
Varsomers794728090
Maprs794728090
PheGenIrs794728090
hapmaprs794728090
1000 genomesrs794728090
hgdprs794728090
ensemblrs794728090
gopubmedrs794728090
geneviewrs794728090
scholarrs794728090
googlers794728090
pharmgkbrs794728090
gwascentralrs794728090
openSNPrs794728090
23andMers794728090
23andMe allrs794728090
SNP Nexus

SNPshotrs794728090
SNPdbers794728090
MSV3drs794728090
GWAS Ctlgrs794728090
Max Magnitude0
ClinVar
Risk rs794728090(G;G)
Alt rs794728090(G;G)
Reference rs794728090(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DSG2-AS1 DSG2
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.29125748C>G
CLNSRC
CLNACC RCV000181230.2,