rs61744449
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs61744449(C;C) |
| Make rs61744449(C;G) |
| Make rs61744449(G;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 16 |
| Position | 30969641 |
| Gene | SETD1A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs61744449 |
| dbSNP (classic) | rs61744449 |
| ClinGen | rs61744449 |
| ebi | rs61744449 |
| HLI | rs61744449 |
| Exac | rs61744449 |
| Gnomad | rs61744449 |
| Varsome | rs61744449 |
| LitVar | rs61744449 |
| Map | rs61744449 |
| PheGenI | rs61744449 |
| Biobank | rs61744449 |
| 1000 genomes | rs61744449 |
| hgdp | rs61744449 |
| ensembl | rs61744449 |
| geneview | rs61744449 |
| scholar | rs61744449 |
| rs61744449 | |
| pharmgkb | rs61744449 |
| gwascentral | rs61744449 |
| openSNP | rs61744449 |
| 23andMe | rs61744449 |
| SNPshot | rs61744449 |
| SNPdbe | rs61744449 |
| MSV3d | rs61744449 |
| GWAS Ctlg | rs61744449 |
| 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 16:30980962_C/T and also as p.R990X
