Rs1143674
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs1143674 |
| hapmap | rs1143674 |
| hgdp | rs1143674 |
| ensembl | rs1143674 |
| gopubmed | rs1143674 |
| scholar | rs1143674 |
| rs1143674 | |
| pharmgkb | rs1143674 |
| hgvbaseg2p | rs1143674 |
| medrefsnp | rs1143674 |
| 23andMe | rs1143674 |
| SNP Nexus |
| Gene | ITGA4 |
| Chromosome | 2 |
| Orientation | plus |
| Position | 182082778 |
| Genotype | Effect |
|---|---|
| rs1143674(A;A) | 1.3x increased autism risk |
| rs1143674(A;G) | 1.3x increased autism risk |
| rs1143674(G;G) | normal |
| Genotypes | Magnitude | Summary |
|---|---|---|
| Rs1143674(A;A) | 1.3x increased autism risk | |
| Rs1143674(A;G) | 1.3x increased autism risk | |
| Rs1143674(G;G) | normal |
rs1143674 is a SNP in the integrin alpha-4 ITGA4 gene on chromosome 2.
Across two sets of family samples (Irish and American), rs1143674 showed a slight association with increased risk for autism, with an odds ratio of 1.3 (p = 0.008). [PMID 18846500]
