rs10500171
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10500171(A;A) |
| Make rs10500171(A;G) |
| Make rs10500171(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 147183313 |
| Gene | CNTNAP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10500171 |
| dbSNP (classic) | rs10500171 |
| ClinGen | rs10500171 |
| ebi | rs10500171 |
| HLI | rs10500171 |
| Exac | rs10500171 |
| Gnomad | rs10500171 |
| Varsome | rs10500171 |
| LitVar | rs10500171 |
| Map | rs10500171 |
| PheGenI | rs10500171 |
| Biobank | rs10500171 |
| 1000 genomes | rs10500171 |
| hgdp | rs10500171 |
| ensembl | rs10500171 |
| geneview | rs10500171 |
| scholar | rs10500171 |
| rs10500171 | |
| pharmgkb | rs10500171 |
| gwascentral | rs10500171 |
| openSNP | rs10500171 |
| 23andMe | rs10500171 |
| SNPshot | rs10500171 |
| SNPdbe | rs10500171 |
| MSV3d | rs10500171 |
| GWAS Ctlg | rs10500171 |
| GMAF | 0.4495 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20414140] Association analysis of CNTNAP2 polymorphisms with autism in the Chinese Han population
