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rs7195303

From SNPedia

Orientationplus
Stabilizedplus
Make rs7195303(A;A)
Make rs7195303(A;G)
Make rs7195303(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position75133681
GeneLOC102723987
is asnp
is mentioned by
dbSNPrs7195303
ebirs7195303
HLIrs7195303
Exacrs7195303
Varsomers7195303
Maprs7195303
PheGenIrs7195303
hapmaprs7195303
1000 genomesrs7195303
hgdprs7195303
ensemblrs7195303
gopubmedrs7195303
geneviewrs7195303
scholarrs7195303
googlers7195303
pharmgkbrs7195303
gwascentralrs7195303
openSNPrs7195303
23andMers7195303
23andMe allrs7195303
SNP Nexus

SNPshotrs7195303
SNPdbers7195303
MSV3drs7195303
GWAS Ctlgrs7195303
GMAF0.1111
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23665963OA-icon.png]
Trait Crohn's disease (time to surgery)
Title Multidimensional prognostic risk assessment identifies association between IL12B variation and surgery in Crohn's disease.
Risk Allele G
P-val 9E-6
Odds Ratio 2.10 [1.5-2.8]