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

rs397516702

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516702(G;T)
Make rs397516702(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position31519873
GeneDSG2
is asnp
is mentioned by
dbSNPrs397516702
ebirs397516702
HLIrs397516702
Exacrs397516702
Varsomers397516702
Maprs397516702
PheGenIrs397516702
hapmaprs397516702
1000 genomesrs397516702
hgdprs397516702
ensemblrs397516702
gopubmedrs397516702
geneviewrs397516702
scholarrs397516702
googlers397516702
pharmgkbrs397516702
gwascentralrs397516702
openSNPrs397516702
23andMers397516702
23andMe allrs397516702
SNP Nexus

SNPshotrs397516702
SNPdbers397516702
MSV3drs397516702
GWAS Ctlgrs397516702
Max Magnitude0
ClinVar
Risk rs397516702(T;T)
Alt rs397516702(T;T)
Reference rs397516702(G;G)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene DSG2
CLNDBN not provided not specified
Reversed 0
HGVS NC_000018.9:g.29099836G>C; NC_000018.9:g.29099836G>T
CLNSRC
CLNACC RCV000181199.1, RCV000037266.3,