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rs794728097

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728097(G;G)
Make rs794728097(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position31542833
GeneDSG2, DSG2-AS1
is asnp
is mentioned by
dbSNPrs794728097
ebirs794728097
HLIrs794728097
Exacrs794728097
Varsomers794728097
Maprs794728097
PheGenIrs794728097
hapmaprs794728097
1000 genomesrs794728097
hgdprs794728097
ensemblrs794728097
gopubmedrs794728097
geneviewrs794728097
scholarrs794728097
googlers794728097
pharmgkbrs794728097
gwascentralrs794728097
openSNPrs794728097
23andMers794728097
23andMe allrs794728097
SNP Nexus

SNPshotrs794728097
SNPdbers794728097
MSV3drs794728097
GWAS Ctlgrs794728097
Max Magnitude0
ClinVar
Risk rs794728097(G;G)
Alt rs794728097(G;G)
Reference rs794728097(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene DSG2-AS1 DSG2
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.29122796T>G
CLNSRC
CLNACC RCV000181249.1,