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rs774863785

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs774863785(A;A)
Make rs774863785(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position31531167
GeneDSG2
is asnp
is mentioned by
dbSNPrs774863785
ebirs774863785
HLIrs774863785
Exacrs774863785
Varsomers774863785
Maprs774863785
PheGenIrs774863785
hapmaprs774863785
1000 genomesrs774863785
hgdprs774863785
ensemblrs774863785
gopubmedrs774863785
geneviewrs774863785
scholarrs774863785
googlers774863785
pharmgkbrs774863785
gwascentralrs774863785
openSNPrs774863785
23andMers774863785
23andMe allrs774863785
SNP Nexus

SNPshotrs774863785
SNPdbers774863785
MSV3drs774863785
GWAS Ctlgrs774863785
Max Magnitude0
ClinVar
Risk rs774863785(A;A)
Alt rs774863785(A;A)
Reference rs774863785(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DSG2
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.29111130G>A
CLNSRC
CLNACC RCV000181216.2,