Rs17883192

From SNPedia

Jump to: navigation, search
is asnp
is mentioned by
dbSNPrs17883192
hapmaprs17883192
hgdprs17883192
ensemblrs17883192
gopubmedrs17883192
scholarrs17883192
googlers17883192
pharmgkbrs17883192
hgvbaseg2prs17883192
medrefsnprs17883192
23andMers17883192
SNP Nexus

GeneIL3RA
Orientationplus
Position1431541
GenotypeEffect
rs17883192(C;C)>3x risk
rs17883192(C;G)3x risk
rs17883192(G;G)common


Genotypes Magnitude Summary
Rs17883192(C;C) >3x risk
Rs17883192(C;G) 3x risk
Rs17883192(G;G) common
rs17883192, part of a haplotype block spanning introns 4, 5 and 6 of the IL3RA gene, has been reported in a whole genome association study to be associated with schizophrenia. (The other SNPs in this block are rs6422441 and rs6603272.)

The risk allele (oriented to the dbSNP entry) is (C); the odds ratio associated with this allele is 3.07. [PMID 17522711]