rs10733648
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10733648(C;C) |
Make rs10733648(C;T) |
Make rs10733648(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 120938501 |
is a | snp |
is | mentioned by |
dbSNP | rs10733648 |
dbSNP (classic) | rs10733648 |
ClinGen | rs10733648 |
ebi | rs10733648 |
HLI | rs10733648 |
Exac | rs10733648 |
Gnomad | rs10733648 |
Varsome | rs10733648 |
LitVar | rs10733648 |
Map | rs10733648 |
PheGenI | rs10733648 |
Biobank | rs10733648 |
1000 genomes | rs10733648 |
hgdp | rs10733648 |
ensembl | rs10733648 |
geneview | rs10733648 |
scholar | rs10733648 |
rs10733648 | |
pharmgkb | rs10733648 |
gwascentral | rs10733648 |
openSNP | rs10733648 |
23andMe | rs10733648 |
SNPshot | rs10733648 |
SNPdbe | rs10733648 |
MSV3d | rs10733648 |
GWAS Ctlg | rs10733648 |
GMAF | 0.3324 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
Rs10733648 | |
---|---|
PubMed | [PMID 17804836] |
Affy Probeset | SNP_A-8603977 |
Affy Orientation | reverse |
On GW 5.0 | 0 |
Alleles A/B | A/G |
Ancestral | C |
Population | |
Allele | T |
Case Freq. | |
Control Freq. | |
Odds Ratio Het | |
Odds Ratio Hom | |
Odds Ratio All | 1.34 |
Disease | Rheumatoid Arthritis (RA) |
rs10733648 is in linkage disequilibrium with a polymorphism that increases susceptibility to Rheumatoid Arthritis 1.34 times for carriers of the T allele [PMID 17804836]