rs4675502
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4675502(A;A) |
| Make rs4675502(A;G) |
| Make rs4675502(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 205221447 |
| Gene | PARD3B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4675502 |
| dbSNP (classic) | rs4675502 |
| ClinGen | rs4675502 |
| ebi | rs4675502 |
| HLI | rs4675502 |
| Exac | rs4675502 |
| Gnomad | rs4675502 |
| Varsome | rs4675502 |
| LitVar | rs4675502 |
| Map | rs4675502 |
| PheGenI | rs4675502 |
| Biobank | rs4675502 |
| 1000 genomes | rs4675502 |
| hgdp | rs4675502 |
| ensembl | rs4675502 |
| geneview | rs4675502 |
| scholar | rs4675502 |
| rs4675502 | |
| pharmgkb | rs4675502 |
| gwascentral | rs4675502 |
| openSNP | rs4675502 |
| 23andMe | rs4675502 |
| SNPshot | rs4675502 |
| SNPdbe | rs4675502 |
| MSV3d | rs4675502 |
| GWAS Ctlg | rs4675502 |
| GMAF | 0.433 |
| 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 | 4E-7 |
| Odds Ratio | 1.28 [1.16-1.41] |
