rs762131795
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs762131795(-;-) |
| Make rs762131795(-;AG) |
| Make rs762131795(AG;AG) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 16 |
| Position | 30966085 |
| Gene | SETD1A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs762131795 |
| dbSNP (classic) | rs762131795 |
| ClinGen | rs762131795 |
| ebi | rs762131795 |
| HLI | rs762131795 |
| Exac | rs762131795 |
| Gnomad | rs762131795 |
| Varsome | rs762131795 |
| LitVar | rs762131795 |
| Map | rs762131795 |
| PheGenI | rs762131795 |
| Biobank | rs762131795 |
| 1000 genomes | rs762131795 |
| hgdp | rs762131795 |
| ensembl | rs762131795 |
| geneview | rs762131795 |
| scholar | rs762131795 |
| rs762131795 | |
| pharmgkb | rs762131795 |
| gwascentral | rs762131795 |
| openSNP | rs762131795 |
| 23andMe | rs762131795 |
| SNPshot | rs762131795 |
| SNPdbe | rs762131795 |
| MSV3d | rs762131795 |
| GWAS Ctlg | rs762131795 |
| 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 16:30977405_CAG/C and also as p.Q735fs
