rs761709838
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs761709838(-;-) |
| Make rs761709838(-;GATG) |
| Make rs761709838(GATG;GATG) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 16 |
| Position | 30958857 |
| Gene | SETD1A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs761709838 |
| dbSNP (classic) | rs761709838 |
| ClinGen | rs761709838 |
| ebi | rs761709838 |
| HLI | rs761709838 |
| Exac | rs761709838 |
| Gnomad | rs761709838 |
| Varsome | rs761709838 |
| LitVar | rs761709838 |
| Map | rs761709838 |
| PheGenI | rs761709838 |
| Biobank | rs761709838 |
| 1000 genomes | rs761709838 |
| hgdp | rs761709838 |
| ensembl | rs761709838 |
| geneview | rs761709838 |
| scholar | rs761709838 |
| rs761709838 | |
| pharmgkb | rs761709838 |
| gwascentral | rs761709838 |
| openSNP | rs761709838 |
| 23andMe | rs761709838 |
| SNPshot | rs761709838 |
| SNPdbe | rs761709838 |
| MSV3d | rs761709838 |
| GWAS Ctlg | rs761709838 |
| Max Magnitude | 0 |
[PMID 26974950
] Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.
referred to in the cited paper as 16:30970178_T/TGATG and also as p.Y42fs
