rs143321486
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs143321486(C;G) |
| Make rs143321486(G;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 17 |
| Position | 42911295 |
| Gene | G6PC |
| is a | snp |
| is | mentioned by |
| dbSNP | rs143321486 |
| dbSNP (classic) | rs143321486 |
| ClinGen | rs143321486 |
| ebi | rs143321486 |
| HLI | rs143321486 |
| Exac | rs143321486 |
| Gnomad | rs143321486 |
| Varsome | rs143321486 |
| LitVar | rs143321486 |
| Map | rs143321486 |
| PheGenI | rs143321486 |
| Biobank | rs143321486 |
| 1000 genomes | rs143321486 |
| hgdp | rs143321486 |
| ensembl | rs143321486 |
| geneview | rs143321486 |
| scholar | rs143321486 |
| rs143321486 | |
| pharmgkb | rs143321486 |
| gwascentral | rs143321486 |
| openSNP | rs143321486 |
| 23andMe | rs143321486 |
| SNPshot | rs143321486 |
| SNPdbe | rs143321486 |
| MSV3d | rs143321486 |
| GWAS Ctlg | rs143321486 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs143321486(G;G) |
| Alt | rs143321486(G;G) |
| Reference | Rs143321486(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | G6PC |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000017.10:g.41063312C>G |
| CLNSRC | |
| CLNACC | RCV000199189.1, |
