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rs212388

From SNPedia

Orientationminus
Stabilizedplus
Make rs212388(A;A)
Make rs212388(A;G)
Make rs212388(G;G)
ReferenceGRCh38 38.1/142
Chromosome6
Position159069404
is asnp
is mentioned by
dbSNPrs212388
ebirs212388
HLIrs212388
Exacrs212388
Varsomers212388
Maprs212388
PheGenIrs212388
hapmaprs212388
1000 genomesrs212388
hgdprs212388
ensemblrs212388
gopubmedrs212388
geneviewrs212388
scholarrs212388
googlers212388
pharmgkbrs212388
gwascentralrs212388
openSNPrs212388
23andMers212388
23andMe allrs212388
SNP Nexus

SNPshotrs212388
SNPdbers212388
MSV3drs212388
GWAS Ctlgrs212388
GMAF0.4486
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21102463OA-icon.png]
Trait
Title Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
Risk Allele G
P-val 2E-11
Odds Ratio 1.1000 [1.05-1.14]
GWAS snp
PMID [PMID 21298027OA-icon.png]
Trait
Title A Meta-Analysis of Genome-Wide Association Scans Identifies IL18RAP, PTPN2, TAGAP, and PUS10 As Shared Risk Loci for Crohn's Disease and Celiac Disease
Risk Allele C
P-val 2E-10
Odds Ratio None None


[PMID 21383967OA-icon.png] Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci.

GWAS snp
PMID [PMID 23128233OA-icon.png]
Trait Crohn's disease
Title Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
Risk Allele C
P-val 3E-14
Odds Ratio 1.11 [1.069-1.141]


[PMID 23044675] Mutation in TAGAP is protective of anal sepsis in ileocolic Crohn's disease.