Have questions? Visit https://www.reddit.com/r/SNPedia

rs794728092

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ATCGT;ATCGT) 0 common in clinvar
Make rs794728092(-;-)
Make rs794728092(-;GTATC)
Make rs794728092(GTATC;GTATC)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position31522160
GeneDSG2
is asnp
is mentioned by
dbSNPrs794728092
dbSNP (old)rs794728092
ClinGenrs794728092
ebirs794728092
HLIrs794728092
Exacrs794728092
Gnomadrs794728092
Varsomers794728092
Maprs794728092
PheGenIrs794728092
Biobankrs794728092
1000 genomesrs794728092
hgdprs794728092
ensemblrs794728092
gopubmedrs794728092
geneviewrs794728092
scholarrs794728092
googlers794728092
pharmgkbrs794728092
gwascentralrs794728092
openSNPrs794728092
23andMers794728092
23andMe allrs794728092
SNP Nexus

SNPshotrs794728092
SNPdbers794728092
MSV3drs794728092
GWAS Ctlgrs794728092
Max Magnitude0
ClinVar
Risk rs794728092(-;-)
Alt rs794728092(-;-)
Reference Rs794728092(ATCGT;ATCGT)
Significance Pathogenic
Disease not provided
Variation info
Gene DSG2
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.29102123_29102127delGTATC
CLNSRC
CLNACC RCV000181239.2,