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rs7900744

From SNPedia

Orientationplus
Stabilizedplus
Make rs7900744(A;A)
Make rs7900744(A;G)
Make rs7900744(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position6023648
GeneIL2RA
is asnp
is mentioned by
dbSNPrs7900744
ebirs7900744
HLIrs7900744
Exacrs7900744
Varsomers7900744
Maprs7900744
PheGenIrs7900744
hapmaprs7900744
1000 genomesrs7900744
hgdprs7900744
ensemblrs7900744
gopubmedrs7900744
geneviewrs7900744
scholarrs7900744
googlers7900744
pharmgkbrs7900744
gwascentralrs7900744
openSNPrs7900744
23andMers7900744
23andMe allrs7900744
SNP Nexus

SNPshotrs7900744
SNPdbers7900744
MSV3drs7900744
GWAS Ctlgrs7900744
GMAF0.2332
Max Magnitude
? (A;A) (A;G) (G;G) 28
Rs7900744
PubMed [PMID 17371467]
Affy Probeset SNP_A-8468428
Affy Orientation same
On GW 5.0 0
Alleles A/B A/G
Ancestral A
Population UK
Allele G
Case Freq.
Control Freq.
Odds Ratio Het
Odds Ratio Hom
Odds Ratio All 1.12
Disease Graves' Disease (GD)


[PMID 17371467] a general susceptibility locus for autoimmune disease found via 1896 Graves' disease patients matched to 1822 controls (P = 4.5 x 10(-4)).

rs7900744 is in linkage disequilibrium with a polymorphism that increases susceptibility to Graves' Disease 1.12 times for carriers of the G allele [PMID 17371467]