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rs373542380

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs373542380(A;A)
Make rs373542380(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position31521111
GeneDSG2
is asnp
is mentioned by
dbSNPrs373542380
ebirs373542380
HLIrs373542380
Exacrs373542380
Varsomers373542380
Maprs373542380
PheGenIrs373542380
hapmaprs373542380
1000 genomesrs373542380
hgdprs373542380
ensemblrs373542380
gopubmedrs373542380
geneviewrs373542380
scholarrs373542380
googlers373542380
pharmgkbrs373542380
gwascentralrs373542380
openSNPrs373542380
23andMers373542380
23andMe allrs373542380
SNP Nexus

SNPshotrs373542380
SNPdbers373542380
MSV3drs373542380
GWAS Ctlgrs373542380
Max Magnitude0
ClinVar
Risk rs373542380(A,T;A,T)
Alt rs373542380(A,T;A,T)
Reference rs373542380(G;G)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene DSG2
CLNDBN not specified
Reversed 0
HGVS NC_000018.9:g.29101074G>A
CLNSRC
CLNACC RCV000037304.3,