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rs802734

From SNPedia

Orientationminus
Stabilizedminus
Make rs802734(C;C)
Make rs802734(C;T)
Make rs802734(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position127957653
is asnp
is mentioned by
dbSNPrs802734
ebirs802734
HLIrs802734
Exacrs802734
Varsomers802734
Maprs802734
PheGenIrs802734
hapmaprs802734
1000 genomesrs802734
hgdprs802734
ensemblrs802734
gopubmedrs802734
geneviewrs802734
scholarrs802734
googlers802734
pharmgkbrs802734
gwascentralrs802734
openSNPrs802734
23andMers802734
23andMe allrs802734
SNP Nexus

SNPshotrs802734
SNPdbers802734
MSV3drs802734
GWAS Ctlgrs802734
GMAF0.1983
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20190752OA-icon.png]
Trait Celiac disease
Title Multiple common variants for celiac disease influencing immune gene expression
Risk Allele G
P-val 3E-14
Odds Ratio 1.17 [1.12-1.22]
GWAS snp
PMID [PMID 21833088OA-icon.png]
Trait
Title Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Risk Allele A
P-val 6E-9
Odds Ratio 1.1000 [1.09-1.12]


[PMID 23820479OA-icon.png] THEMIS and PTPRK in celiac intestinal mucosa: coexpression in disease and after in vitro gliadin challenge.