rs141600901
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs141600901(-;-) |
| Make rs141600901(-;AC) |
| Make rs141600901(AC;AC) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 15 |
| Position | 48739003 |
| Gene | CEP152 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs141600901 |
| dbSNP (classic) | rs141600901 |
| ClinGen | rs141600901 |
| ebi | rs141600901 |
| HLI | rs141600901 |
| Exac | rs141600901 |
| Gnomad | rs141600901 |
| Varsome | rs141600901 |
| LitVar | rs141600901 |
| Map | rs141600901 |
| PheGenI | rs141600901 |
| Biobank | rs141600901 |
| 1000 genomes | rs141600901 |
| hgdp | rs141600901 |
| ensembl | rs141600901 |
| geneview | rs141600901 |
| scholar | rs141600901 |
| rs141600901 | |
| pharmgkb | rs141600901 |
| gwascentral | rs141600901 |
| openSNP | rs141600901 |
| 23andMe | rs141600901 |
| SNPshot | rs141600901 |
| SNPdbe | rs141600901 |
| MSV3d | rs141600901 |
| GWAS Ctlg | rs141600901 |
| Max Magnitude | 0 |
OMIM pathogenic variant
