rs145229472
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs145229472(A;A) |
| Make rs145229472(A;C) |
| Make rs145229472(C;C) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 11 |
| Position | 108146200 |
| Gene | ACAT1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs145229472 |
| dbSNP (classic) | rs145229472 |
| ClinGen | rs145229472 |
| ebi | rs145229472 |
| HLI | rs145229472 |
| Exac | rs145229472 |
| Gnomad | rs145229472 |
| Varsome | rs145229472 |
| LitVar | rs145229472 |
| Map | rs145229472 |
| PheGenI | rs145229472 |
| Biobank | rs145229472 |
| 1000 genomes | rs145229472 |
| hgdp | rs145229472 |
| ensembl | rs145229472 |
| geneview | rs145229472 |
| scholar | rs145229472 |
| rs145229472 | |
| pharmgkb | rs145229472 |
| gwascentral | rs145229472 |
| openSNP | rs145229472 |
| 23andMe | rs145229472 |
| SNPshot | rs145229472 |
| SNPdbe | rs145229472 |
| MSV3d | rs145229472 |
| GWAS Ctlg | rs145229472 |
| Max Magnitude | 0 |
OMIM pathogenic variant
