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rs10733648

From SNPedia

Orientationplus
Stabilizedplus
Make rs10733648(C;C)
Make rs10733648(C;T)
Make rs10733648(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position120938501
is asnp
is mentioned by
dbSNPrs10733648
ebirs10733648
HLIrs10733648
Exacrs10733648
Varsomers10733648
Maprs10733648
PheGenIrs10733648
hapmaprs10733648
1000 genomesrs10733648
hgdprs10733648
ensemblrs10733648
gopubmedrs10733648
geneviewrs10733648
scholarrs10733648
googlers10733648
pharmgkbrs10733648
gwascentralrs10733648
openSNPrs10733648
23andMers10733648
23andMe allrs10733648
SNP Nexus

SNPshotrs10733648
SNPdbers10733648
MSV3drs10733648
GWAS Ctlgrs10733648
GMAF0.3324
Max Magnitude
? (C;C) (C;T) (T;T) 28
Rs10733648
PubMed [PMID 17804836OA-icon.png]
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 17804836OA-icon.png]