rs10497655
From SNPedia
| Orientation | plus |
| Make rs10497655(C;C) |
| Make rs10497655(C;T) |
| Make rs10497655(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 2 |
| Position | 184597314 |
| Gene | LOC105373780, ZNF804A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10497655 |
| dbSNP (classic) | rs10497655 |
| ClinGen | rs10497655 |
| ebi | rs10497655 |
| HLI | rs10497655 |
| Exac | rs10497655 |
| Gnomad | rs10497655 |
| Varsome | rs10497655 |
| LitVar | rs10497655 |
| Map | rs10497655 |
| PheGenI | rs10497655 |
| Biobank | rs10497655 |
| 1000 genomes | rs10497655 |
| hgdp | rs10497655 |
| ensembl | rs10497655 |
| geneview | rs10497655 |
| scholar | rs10497655 |
| rs10497655 | |
| pharmgkb | rs10497655 |
| gwascentral | rs10497655 |
| openSNP | rs10497655 |
| 23andMe | rs10497655 |
| SNPshot | rs10497655 |
| SNPdbe | rs10497655 |
| MSV3d | rs10497655 |
| GWAS Ctlg | rs10497655 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 30670685
] A promoter variant in ZNF804A decreasing its expression increases the risk of autism spectrum disorder in the Han Chinese population.
