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rs2006996

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs2006996(C;C)
Make rs2006996(C;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position114830358
is asnp
is mentioned by
dbSNPrs2006996
ebirs2006996
HLIrs2006996
Exacrs2006996
Varsomers2006996
Maprs2006996
PheGenIrs2006996
hapmaprs2006996
1000 genomesrs2006996
hgdprs2006996
ensemblrs2006996
gopubmedrs2006996
geneviewrs2006996
scholarrs2006996
googlers2006996
pharmgkbrs2006996
gwascentralrs2006996
openSNPrs2006996
23andMers2006996
23andMe allrs2006996
SNP Nexus

SNPshotrs2006996
SNPdbers2006996
MSV3drs2006996
GWAS Ctlgrs2006996
GMAF0.141
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21699788]
Trait
Title HLA-Cw*1202-B*5201-DRB1*1502 Haplotype Increases Risk for Ulcerative Colitis But Reduces Risk for Crohn's Disease.
Risk Allele T
P-val 4E-13
Odds Ratio 1.6700 [1.47-1.92]