rs7900744
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7900744(A;A) |
Make rs7900744(A;G) |
Make rs7900744(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 6023648 |
Gene | IL2RA |
is a | snp |
is | mentioned by |
dbSNP | rs7900744 |
dbSNP (classic) | rs7900744 |
ClinGen | rs7900744 |
ebi | rs7900744 |
HLI | rs7900744 |
Exac | rs7900744 |
Gnomad | rs7900744 |
Varsome | rs7900744 |
LitVar | rs7900744 |
Map | rs7900744 |
PheGenI | rs7900744 |
Biobank | rs7900744 |
1000 genomes | rs7900744 |
hgdp | rs7900744 |
ensembl | rs7900744 |
geneview | rs7900744 |
scholar | rs7900744 |
rs7900744 | |
pharmgkb | rs7900744 |
gwascentral | rs7900744 |
openSNP | rs7900744 |
23andMe | rs7900744 |
SNPshot | rs7900744 |
SNPdbe | rs7900744 |
MSV3d | rs7900744 |
GWAS Ctlg | rs7900744 |
GMAF | 0.2332 |
Max Magnitude | 0 |
? | (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]