rs779565865
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs779565865(-;-) |
| Make rs779565865(-;C) |
| Make rs779565865(C;C) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 11 |
| Position | 108133848 |
| Gene | ACAT1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs779565865 |
| dbSNP (classic) | rs779565865 |
| ClinGen | rs779565865 |
| ebi | rs779565865 |
| HLI | rs779565865 |
| Exac | rs779565865 |
| Gnomad | rs779565865 |
| Varsome | rs779565865 |
| LitVar | rs779565865 |
| Map | rs779565865 |
| PheGenI | rs779565865 |
| Biobank | rs779565865 |
| 1000 genomes | rs779565865 |
| hgdp | rs779565865 |
| ensembl | rs779565865 |
| geneview | rs779565865 |
| scholar | rs779565865 |
| rs779565865 | |
| pharmgkb | rs779565865 |
| gwascentral | rs779565865 |
| openSNP | rs779565865 |
| 23andMe | rs779565865 |
| SNPshot | rs779565865 |
| SNPdbe | rs779565865 |
| MSV3d | rs779565865 |
| GWAS Ctlg | rs779565865 |
| Max Magnitude | 0 |
aka NM_000019.3(ACAT1):c.149delC or (p.Thr50Asnfs)
OMIM pathogenic variant
