Rs11362

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is asnp
is mentioned by
dbSNPrs11362
hapmaprs11362
hgdprs11362
ensemblrs11362
gopubmedrs11362
scholarrs11362
googlers11362
pharmgkbrs11362
hgvbaseg2prs11362
medrefsnprs11362
23andMers11362
SNP Nexus

GeneDEFB1
Chromosome8
Orientationminus
Position6722808
GenotypeEffect
rs11362(A;A)normal risk
rs11362(A;G)2.4x increased risk for one form of Crohn's disease
rs11362(G;G)normal risk


Genotypes Magnitude Summary
Rs11362(A;A) 00 normal risk
Rs11362(A;G) 2.4x increased risk for one form of Crohn's disease
Rs11362(C;C) 00
Rs11362(G;G) 00 normal risk
Rs11362(T;T) 00
Heterozygotes for SNP rs11362, located in the DEFB1 gene, are reported to be at increased risk for colonic Crohn's disease - but not the ileal or ileocolonic forms of the disease - based on a study of 190 Caucasians. The odds ratio is 2.393 (CI: 1.18-4.87, p=0.02).[PMID 17943629]

[PMID 18938660] G-20A rs11362(A;G) 2.4x risk colonic and ileocolonic Crohn's disease but no association was detected for the ileal localization

Neighborrs1800972
Distance24
? (A;A) (A;G) (G;G)


[PMID 19460328] SNP 668C (-44) alters a NF-kappaB1 putative binding site in non-coding strand of human beta-defensin 1 (DEFB1) and is associated with lepromatous leprosy