rs34714481
From SNPedia
| Orientation | plus |
| Make rs34714481(A;A) |
| Make rs34714481(A;G) |
| Make rs34714481(G;G) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 2 |
| Position | 184597742 |
| Gene | LOC105373780, ZNF804A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs34714481 |
| dbSNP (classic) | rs34714481 |
| ClinGen | rs34714481 |
| ebi | rs34714481 |
| HLI | rs34714481 |
| Exac | rs34714481 |
| Gnomad | rs34714481 |
| Varsome | rs34714481 |
| LitVar | rs34714481 |
| Map | rs34714481 |
| PheGenI | rs34714481 |
| Biobank | rs34714481 |
| 1000 genomes | rs34714481 |
| hgdp | rs34714481 |
| ensembl | rs34714481 |
| geneview | rs34714481 |
| scholar | rs34714481 |
| rs34714481 | |
| pharmgkb | rs34714481 |
| gwascentral | rs34714481 |
| openSNP | rs34714481 |
| 23andMe | rs34714481 |
| SNPshot | rs34714481 |
| SNPdbe | rs34714481 |
| MSV3d | rs34714481 |
| GWAS Ctlg | rs34714481 |
| Max Magnitude | 0 |
[PMID 30670685
] A promoter variant in ZNF804A decreasing its expression increases the risk of autism spectrum disorder in the Han Chinese population.
