rs769183311
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs769183311(C;T) |
| Make rs769183311(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 8 |
| Position | 98140867 |
| Gene | POP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs769183311 |
| dbSNP (classic) | rs769183311 |
| ClinGen | rs769183311 |
| ebi | rs769183311 |
| HLI | rs769183311 |
| Exac | rs769183311 |
| Gnomad | rs769183311 |
| Varsome | rs769183311 |
| LitVar | rs769183311 |
| Map | rs769183311 |
| PheGenI | rs769183311 |
| Biobank | rs769183311 |
| 1000 genomes | rs769183311 |
| hgdp | rs769183311 |
| ensembl | rs769183311 |
| geneview | rs769183311 |
| scholar | rs769183311 |
| rs769183311 | |
| pharmgkb | rs769183311 |
| gwascentral | rs769183311 |
| openSNP | rs769183311 |
| 23andMe | rs769183311 |
| SNPshot | rs769183311 |
| SNPdbe | rs769183311 |
| MSV3d | rs769183311 |
| GWAS Ctlg | rs769183311 |
| Max Magnitude | 0 |
aka NM_001145860.1(POP1):c.1573C>T or (p.Pro525Ser)
OMIM pathogenic variant
