rs772727116
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs772727116(C;T) |
| Make rs772727116(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 19 |
| Position | 49862408 |
| Gene | PNKP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs772727116 |
| dbSNP (classic) | rs772727116 |
| ClinGen | rs772727116 |
| ebi | rs772727116 |
| HLI | rs772727116 |
| Exac | rs772727116 |
| Gnomad | rs772727116 |
| Varsome | rs772727116 |
| LitVar | rs772727116 |
| Map | rs772727116 |
| PheGenI | rs772727116 |
| Biobank | rs772727116 |
| 1000 genomes | rs772727116 |
| hgdp | rs772727116 |
| ensembl | rs772727116 |
| geneview | rs772727116 |
| scholar | rs772727116 |
| rs772727116 | |
| pharmgkb | rs772727116 |
| gwascentral | rs772727116 |
| openSNP | rs772727116 |
| 23andMe | rs772727116 |
| SNPshot | rs772727116 |
| SNPdbe | rs772727116 |
| MSV3d | rs772727116 |
| GWAS Ctlg | rs772727116 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs772727116(T;T) |
| Alt | rs772727116(T;T) |
| Reference | Rs772727116(C;C) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | PNKP |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000019.9:g.50365665C>T |
| CLNSRC | |
| CLNACC | RCV000188442.2, |
