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rs794728083

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728083(C;T)
Make rs794728083(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position31524526
GeneDSG2
is asnp
is mentioned by
dbSNPrs794728083
ebirs794728083
HLIrs794728083
Exacrs794728083
Varsomers794728083
Maprs794728083
PheGenIrs794728083
hapmaprs794728083
1000 genomesrs794728083
hgdprs794728083
ensemblrs794728083
gopubmedrs794728083
geneviewrs794728083
scholarrs794728083
googlers794728083
pharmgkbrs794728083
gwascentralrs794728083
openSNPrs794728083
23andMers794728083
23andMe allrs794728083
SNP Nexus

SNPshotrs794728083
SNPdbers794728083
MSV3drs794728083
GWAS Ctlgrs794728083
Max Magnitude0
ClinVar
Risk rs794728083(T;T)
Alt rs794728083(T;T)
Reference rs794728083(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene DSG2
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.29104489C>T
CLNSRC
CLNACC RCV000181208.1,