rs10244837
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10244837(A;A) |
| Make rs10244837(A;G) |
| Make rs10244837(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 146778222 |
| Gene | CNTNAP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10244837 |
| dbSNP (classic) | rs10244837 |
| ClinGen | rs10244837 |
| ebi | rs10244837 |
| HLI | rs10244837 |
| Exac | rs10244837 |
| Gnomad | rs10244837 |
| Varsome | rs10244837 |
| LitVar | rs10244837 |
| Map | rs10244837 |
| PheGenI | rs10244837 |
| Biobank | rs10244837 |
| 1000 genomes | rs10244837 |
| hgdp | rs10244837 |
| ensembl | rs10244837 |
| geneview | rs10244837 |
| scholar | rs10244837 |
| rs10244837 | |
| pharmgkb | rs10244837 |
| gwascentral | rs10244837 |
| openSNP | rs10244837 |
| 23andMe | rs10244837 |
| SNPshot | rs10244837 |
| SNPdbe | rs10244837 |
| MSV3d | rs10244837 |
| GWAS Ctlg | rs10244837 |
| GMAF | 0.4545 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20414140] Association analysis of CNTNAP2 polymorphisms with autism in the Chinese Han population
