rs6872664
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6872664(C;C) |
| Make rs6872664(C;T) |
| Make rs6872664(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 135031908 |
| Gene | C5orf66, PITX1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6872664 |
| dbSNP (classic) | rs6872664 |
| ClinGen | rs6872664 |
| ebi | rs6872664 |
| HLI | rs6872664 |
| Exac | rs6872664 |
| Gnomad | rs6872664 |
| Varsome | rs6872664 |
| LitVar | rs6872664 |
| Map | rs6872664 |
| PheGenI | rs6872664 |
| Biobank | rs6872664 |
| 1000 genomes | rs6872664 |
| hgdp | rs6872664 |
| ensembl | rs6872664 |
| geneview | rs6872664 |
| scholar | rs6872664 |
| rs6872664 | |
| pharmgkb | rs6872664 |
| gwascentral | rs6872664 |
| openSNP | rs6872664 |
| 23andMe | rs6872664 |
| SNPshot | rs6872664 |
| SNPdbe | rs6872664 |
| MSV3d | rs6872664 |
| GWAS Ctlg | rs6872664 |
| GMAF | 0.1598 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
mentioned by gs240[PMID 18053270
] Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysis.
[PMID 20678243] Assessing the impact of a combined analysis of four common low-risk genetic variants on autism risk.
[PMID 22739633] The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families
