Rs7807268

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is asnp
is mentioned by
dbSNPrs7807268
hapmaprs7807268
hgdprs7807268
ensemblrs7807268
gopubmedrs7807268
scholarrs7807268
googlers7807268
pharmgkbrs7807268
hgvbaseg2prs7807268
medrefsnprs7807268
23andMers7807268
SNP Nexus

Chromosome7
Orientationplus
Position147888980
GenotypeEffect
rs7807268(C;C)1.4x risk
rs7807268(C;G)1.3x risk
rs7807268(G;G)normal


Genotypes Magnitude Summary
Rs7807268(C;C) 00 1.4x risk
Rs7807268(C;G) 1.3x risk
Rs7807268(G;G) normal
rs7807268 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 1.38 (CI 1.20-1.60), and for homozygotes, 1.47 (CI 1.24-1.74). [PMID 17554300]

  • Note: there is a slight amount of ambiguity over the orientation of this SNP information relative to the dbSNP entry.
? (C;C) (C;G) (G;G)