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rs200804638

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200804638(C;T)
Make rs200804638(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position31541198
GeneDSG2
is asnp
is mentioned by
dbSNPrs200804638
ebirs200804638
HLIrs200804638
Exacrs200804638
Varsomers200804638
Maprs200804638
PheGenIrs200804638
hapmaprs200804638
1000 genomesrs200804638
hgdprs200804638
ensemblrs200804638
gopubmedrs200804638
geneviewrs200804638
scholarrs200804638
googlers200804638
pharmgkbrs200804638
gwascentralrs200804638
openSNPrs200804638
23andMers200804638
23andMe allrs200804638
SNP Nexus

SNPshotrs200804638
SNPdbers200804638
MSV3drs200804638
GWAS Ctlgrs200804638
Max Magnitude0
ClinVar
Risk rs200804638(T;T)
Alt rs200804638(T;T)
Reference rs200804638(C;C)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene DSG2
CLNDBN not provided not specified
Reversed 0
HGVS NC_000018.9:g.29121161C>T
CLNSRC
CLNACC RCV000181226.1, RCV000223710.1,