rs754369980
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs754369980(-;-) |
| Make rs754369980(-;C) |
| Make rs754369980(C;C) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 16 |
| Position | 30965995 |
| Gene | SETD1A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs754369980 |
| dbSNP (classic) | rs754369980 |
| ClinGen | rs754369980 |
| ebi | rs754369980 |
| HLI | rs754369980 |
| Exac | rs754369980 |
| Gnomad | rs754369980 |
| Varsome | rs754369980 |
| LitVar | rs754369980 |
| Map | rs754369980 |
| PheGenI | rs754369980 |
| Biobank | rs754369980 |
| 1000 genomes | rs754369980 |
| hgdp | rs754369980 |
| ensembl | rs754369980 |
| geneview | rs754369980 |
| scholar | rs754369980 |
| rs754369980 | |
| pharmgkb | rs754369980 |
| gwascentral | rs754369980 |
| openSNP | rs754369980 |
| 23andMe | rs754369980 |
| SNPshot | rs754369980 |
| SNPdbe | rs754369980 |
| MSV3d | rs754369980 |
| GWAS Ctlg | rs754369980 |
| 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 16:30977316_G/GC and also as p.G705fs
