rs966888627
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs966888627(C;C) |
| Make rs966888627(C;T) |
| Make rs966888627(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 15 |
| Position | 48797660 |
| Gene | CEP152 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs966888627 |
| dbSNP (classic) | rs966888627 |
| ClinGen | rs966888627 |
| ebi | rs966888627 |
| HLI | rs966888627 |
| Exac | rs966888627 |
| Gnomad | rs966888627 |
| Varsome | rs966888627 |
| LitVar | rs966888627 |
| Map | rs966888627 |
| PheGenI | rs966888627 |
| Biobank | rs966888627 |
| 1000 genomes | rs966888627 |
| hgdp | rs966888627 |
| ensembl | rs966888627 |
| geneview | rs966888627 |
| scholar | rs966888627 |
| rs966888627 | |
| pharmgkb | rs966888627 |
| gwascentral | rs966888627 |
| openSNP | rs966888627 |
| 23andMe | rs966888627 |
| SNPshot | rs966888627 |
| SNPdbe | rs966888627 |
| MSV3d | rs966888627 |
| GWAS Ctlg | rs966888627 |
| Max Magnitude | 0 |
aka NM_001194998.1(CEP152):c.261+1G>C
OMIM pathogenic variant
