rs7711337
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7711337(A;A) |
| Make rs7711337(A;G) |
| Make rs7711337(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 162656512 |
| Gene | LOC105377698 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7711337 |
| dbSNP (classic) | rs7711337 |
| ClinGen | rs7711337 |
| ebi | rs7711337 |
| HLI | rs7711337 |
| Exac | rs7711337 |
| Gnomad | rs7711337 |
| Varsome | rs7711337 |
| LitVar | rs7711337 |
| Map | rs7711337 |
| PheGenI | rs7711337 |
| Biobank | rs7711337 |
| 1000 genomes | rs7711337 |
| hgdp | rs7711337 |
| ensembl | rs7711337 |
| geneview | rs7711337 |
| scholar | rs7711337 |
| rs7711337 | |
| pharmgkb | rs7711337 |
| gwascentral | rs7711337 |
| openSNP | rs7711337 |
| 23andMe | rs7711337 |
| SNPshot | rs7711337 |
| SNPdbe | rs7711337 |
| MSV3d | rs7711337 |
| GWAS Ctlg | rs7711337 |
| GMAF | 0.3402 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22843504 ]
|
| Trait | Autism |
| Title | Individual common variants exert weak effects on the risk for autism spectrum disorderspi. |
| Risk Allele | |
| P-val | 8E-7 |
| Odds Ratio | 1.22 [1.12-1.32] |
