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rs9792269

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs9792269(A;G)
Make rs9792269(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position128252343
is asnp
is mentioned by
dbSNPrs9792269
ebirs9792269
HLIrs9792269
Exacrs9792269
Varsomers9792269
Maprs9792269
PheGenIrs9792269
hapmaprs9792269
1000 genomesrs9792269
hgdprs9792269
ensemblrs9792269
gopubmedrs9792269
geneviewrs9792269
scholarrs9792269
googlers9792269
pharmgkbrs9792269
gwascentralrs9792269
openSNPrs9792269
23andMers9792269
23andMe allrs9792269
SNP Nexus

SNPshotrs9792269
SNPdbers9792269
MSV3drs9792269
GWAS Ctlgrs9792269
GMAF0.1786
Max Magnitude0
? (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 3E-9
Odds Ratio 1.14 [1.10-1.19]