Rs10210302

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is asnp
is mentioned by
dbSNPrs10210302
hapmaprs10210302
hgdprs10210302
ensemblrs10210302
gopubmedrs10210302
scholarrs10210302
googlers10210302
pharmgkbrs10210302
hgvbaseg2prs10210302
medrefsnprs10210302
23andMers10210302
SNP Nexus

GeneATG16L1
Chromosome2
Orientationplus
Position233823577
GenotypeEffect
rs10210302(T;T)1.8x risk
rs10210302(C;T)1.2x risk
rs10210302(C;C)normal


Genotypes Magnitude Summary
Rs10210302(C;C) 00 normal
Rs10210302(C;T) 1.2x risk
Rs10210302(T;T) 1.8x risk
rs10210302 has been reported in a large study to be associated with Crohn's disease.

The risk allele (oriented to the dbSNP entry) is (T); the odds ratio associated with heterozygotes is 1.19 (CI 1.01-1.41), and for homozygotes, 1.85 (CI 1.56-2.21). [PMID 17554300]

? (C;C) (C;T) (T;T)
Related to INFLAMMATORY BOWEL DISEASE 10; IBD10 according to omim 611081. See also