Rs11833579

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is asnp
is mentioned by
dbSNPrs11833579
hapmaprs11833579
hgdprs11833579
ensemblrs11833579
gopubmedrs11833579
scholarrs11833579
googlers11833579
pharmgkbrs11833579
hgvbaseg2prs11833579
medrefsnprs11833579
23andMers11833579
SNP Nexus

GeneNINJ2
Chromosome12
Orientationplus
Position645459
GenotypeEffect
rs11833579(A;A)1.6x increased risk for stroke
rs11833579(A;G)1.3x increased risk for stroke
rs11833579(G;G)normal


Genotypes Magnitude Summary
Rs11833579(A;A) 2.42.4 1.6x increased risk for stroke
Rs11833579(A;G) 2.22.2 1.3x increased risk for stroke
Rs11833579(G;G) 00 normal
rs11833579 is one of 2 SNPs found near the NINJ2 gene on chromosome 12 associated with increased risk for both total stroke and ischemic stroke, based on a large study of four cohorts including both blacks and whites. The other (linked) SNP is rs12425791.

Results of this 20,000+ person study suggested that each minor (risk) allele at these two SNPs increases the hazard ratio for total stroke about 1.31 (CI: 1.19 - 1.44) and for ischemic stroke by about 1.40 (CI: 1.27 - 1.56). The corresponding population attributable risks were 11 to 13% for total stroke and 14 to 17% for ischemic stroke, which is fairly high for this sort of SNP. 10.1056/NEJMoa0900094

? (A;A) (A;G) (G;G)