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rs10903122

From SNPedia

Orientationplus
Stabilizedplus
Make rs10903122(A;A)
Make rs10903122(A;G)
Make rs10903122(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position24977085
is asnp
is mentioned by
dbSNPrs10903122
ebirs10903122
HLIrs10903122
Exacrs10903122
Varsomers10903122
Maprs10903122
PheGenIrs10903122
hapmaprs10903122
1000 genomesrs10903122
hgdprs10903122
ensemblrs10903122
gopubmedrs10903122
geneviewrs10903122
scholarrs10903122
googlers10903122
pharmgkbrs10903122
gwascentralrs10903122
openSNPrs10903122
23andMers10903122
23andMe allrs10903122
SNP Nexus

SNPshotrs10903122
SNPdbers10903122
MSV3drs10903122
GWAS Ctlgrs10903122
GMAF0.3825
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20190752OA-icon.png]
Trait Celiac disease
Title Multiple common variants for celiac disease influencing immune gene expression
Risk Allele
P-val 2E-10
Odds Ratio 1.12 [1.09-1.18]