rs11959298
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11959298(A;A) |
| Make rs11959298(A;G) |
| Make rs11959298(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 135031850 |
| Gene | C5orf66, PITX1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11959298 |
| dbSNP (classic) | rs11959298 |
| ClinGen | rs11959298 |
| ebi | rs11959298 |
| HLI | rs11959298 |
| Exac | rs11959298 |
| Gnomad | rs11959298 |
| Varsome | rs11959298 |
| LitVar | rs11959298 |
| Map | rs11959298 |
| PheGenI | rs11959298 |
| Biobank | rs11959298 |
| 1000 genomes | rs11959298 |
| hgdp | rs11959298 |
| ensembl | rs11959298 |
| geneview | rs11959298 |
| scholar | rs11959298 |
| rs11959298 | |
| pharmgkb | rs11959298 |
| gwascentral | rs11959298 |
| openSNP | rs11959298 |
| 23andMe | rs11959298 |
| SNPshot | rs11959298 |
| SNPdbe | rs11959298 |
| MSV3d | rs11959298 |
| GWAS Ctlg | rs11959298 |
| GMAF | 0.202 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 18053270
] Individuals homozygous or heterozygous for the rs11959298(A)-rs6596189(C) haplotype risk allele were 2.54 and 1.59 fold more likely to have autism, respectively, compared to rs11959298(G)-rs6596189(T) carriers.
Note/caveat emptor: ~90% of the world's population carries what the authors from this for-profit genetic testing company call the "risk haplotype", yet the frequency of autism is less than 1% (perhaps 1 in 150).
