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rs10790268

From SNPedia

Orientationplus
Stabilizedplus
Make rs10790268(A;A)
Make rs10790268(A;G)
Make rs10790268(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position118858682
is asnp
is mentioned by
dbSNPrs10790268
dbSNP (classic)rs10790268
ClinGenrs10790268
ebirs10790268
HLIrs10790268
Exacrs10790268
Gnomadrs10790268
Varsomers10790268
LitVarrs10790268
Maprs10790268
PheGenIrs10790268
Biobankrs10790268
1000 genomesrs10790268
hgdprs10790268
ensemblrs10790268
geneviewrs10790268
scholarrs10790268
googlers10790268
pharmgkbrs10790268
gwascentralrs10790268
openSNPrs10790268
23andMers10790268
SNPshotrs10790268
SNPdbers10790268
MSV3drs10790268
GWAS Ctlgrs10790268
Max Magnitude0
GWAS snp
PMID [PMID 24390342OA-icon.png]
Trait Rheumatoid arthritis
Title Genetics of rheumatoid arthritis contributes to biology and drug discovery.
Risk Allele G
P-val 1E-17
Odds Ratio 1.17 [1.13-1.22]