rs767645983
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs767645983(G;G) |
| Make rs767645983(G;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 19 |
| Position | 49861883 |
| Gene | PNKP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs767645983 |
| dbSNP (classic) | rs767645983 |
| ClinGen | rs767645983 |
| ebi | rs767645983 |
| HLI | rs767645983 |
| Exac | rs767645983 |
| Gnomad | rs767645983 |
| Varsome | rs767645983 |
| LitVar | rs767645983 |
| Map | rs767645983 |
| PheGenI | rs767645983 |
| Biobank | rs767645983 |
| 1000 genomes | rs767645983 |
| hgdp | rs767645983 |
| ensembl | rs767645983 |
| geneview | rs767645983 |
| scholar | rs767645983 |
| rs767645983 | |
| pharmgkb | rs767645983 |
| gwascentral | rs767645983 |
| openSNP | rs767645983 |
| 23andMe | rs767645983 |
| SNPshot | rs767645983 |
| SNPdbe | rs767645983 |
| MSV3d | rs767645983 |
| GWAS Ctlg | rs767645983 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs767645983(G;G) |
| Alt | rs767645983(G;G) |
| Reference | Rs767645983(T;T) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | PNKP |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000019.9:g.50365140T>G |
| CLNSRC | |
| CLNACC | RCV000188450.1, |
