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rs17883192

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) >3x risk
(C;G) 3x risk
(G;G) common
ReferenceGRCh38 38.1/141
ChromosomeX
Position1352649
GeneIL3RA, LOC101928055
is asnp
is mentioned by
dbSNPrs17883192
ebirs17883192
HLIrs17883192
Exacrs17883192
Varsomers17883192
Maprs17883192
PheGenIrs17883192
hapmaprs17883192
1000 genomesrs17883192
hgdprs17883192
ensemblrs17883192
gopubmedrs17883192
geneviewrs17883192
scholarrs17883192
googlers17883192
pharmgkbrs17883192
gwascentralrs17883192
openSNPrs17883192
23andMers17883192
23andMe allrs17883192
SNP Nexus

SNPshotrs17883192
SNPdbers17883192
MSV3drs17883192
GWAS Ctlgrs17883192
GMAF0.3039
Max Magnitude
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]