Rs8111071

From SNPedia

Jump to: navigation, search
is asnp
is mentioned by
dbSNPrs8111071
hapmaprs8111071
hgdprs8111071
ensemblrs8111071
gopubmedrs8111071
scholarrs8111071
googlers8111071
pharmgkbrs8111071
hgvbaseg2prs8111071
medrefsnprs8111071
23andMers8111071
SNP Nexus

GeneRSHL1
Chromosome19
Orientationplus
Position50999245
GenotypeEffect
rs8111071(A;A)1.3x risk
rs8111071(A;G)1.5x risk
rs8111071(G;G)normal


Genotypes Magnitude Summary
Rs8111071(A;A) 00 1.3x risk
Rs8111071(A;G) 1.5x risk
Rs8111071(G;G) normal
rs8111071 has been reported in a large study to be associated with Crohn's disease.

The risk allele (oriented to the dbSNP entry) is (G); the odds ratio associated with heterozygotes is 1.47 (CI 1.25-1.73), and for homozygotes, 1.28 (CI 0.56-2.88). [PMID 17554300]

? (G;G) (A;A) (A;G)