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rs751012696

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs751012696(A;A)
Make rs751012696(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position31524763
GeneDSG2
is asnp
is mentioned by
dbSNPrs751012696
ebirs751012696
HLIrs751012696
Exacrs751012696
Varsomers751012696
Maprs751012696
PheGenIrs751012696
hapmaprs751012696
1000 genomesrs751012696
hgdprs751012696
ensemblrs751012696
gopubmedrs751012696
geneviewrs751012696
scholarrs751012696
googlers751012696
pharmgkbrs751012696
gwascentralrs751012696
openSNPrs751012696
23andMers751012696
23andMe allrs751012696
SNP Nexus

SNPshotrs751012696
SNPdbers751012696
MSV3drs751012696
GWAS Ctlgrs751012696
Max Magnitude0
ClinVar
Risk rs751012696(A;A)
Alt rs751012696(A;A)
Reference rs751012696(G;G)
Significance Pathogenic
Disease not specified
Variation info
Gene DSG2
CLNDBN not specified
Reversed 0
HGVS NC_000018.9:g.29104726G>A
CLNSRC
CLNACC RCV000181212.2,