rs1718101
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 |
| Make rs1718101(A;A) |
| Make rs1718101(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 146425696 |
| Gene | CNTNAP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1718101 |
| dbSNP (classic) | rs1718101 |
| ClinGen | rs1718101 |
| ebi | rs1718101 |
| HLI | rs1718101 |
| Exac | rs1718101 |
| Gnomad | rs1718101 |
| Varsome | rs1718101 |
| LitVar | rs1718101 |
| Map | rs1718101 |
| PheGenI | rs1718101 |
| Biobank | rs1718101 |
| 1000 genomes | rs1718101 |
| hgdp | rs1718101 |
| ensembl | rs1718101 |
| geneview | rs1718101 |
| scholar | rs1718101 |
| rs1718101 | |
| pharmgkb | rs1718101 |
| gwascentral | rs1718101 |
| openSNP | rs1718101 |
| 23andMe | rs1718101 |
| SNPshot | rs1718101 |
| SNPdbe | rs1718101 |
| MSV3d | rs1718101 |
| GWAS Ctlg | rs1718101 |
| GMAF | 0.02204 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 22843504
] Individual common variants exert weak effects on risk for Autism Spectrum Disorders
