rs34028295
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (-;-) | 0 | common in clinvar |
| (I;I) | 0 | miscall by 23andMe; you have the normal genotype |
| Make rs34028295(-;G) |
| Make rs34028295(G;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 12 |
| Position | 50120124 |
| Gene | COX14 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs34028295 |
| dbSNP (classic) | rs34028295 |
| ClinGen | rs34028295 |
| ebi | rs34028295 |
| HLI | rs34028295 |
| Exac | rs34028295 |
| Gnomad | rs34028295 |
| Varsome | rs34028295 |
| LitVar | rs34028295 |
| Map | rs34028295 |
| PheGenI | rs34028295 |
| Biobank | rs34028295 |
| 1000 genomes | rs34028295 |
| hgdp | rs34028295 |
| ensembl | rs34028295 |
| geneview | rs34028295 |
| scholar | rs34028295 |
| rs34028295 | |
| pharmgkb | rs34028295 |
| gwascentral | rs34028295 |
| openSNP | rs34028295 |
| 23andMe | rs34028295 |
| SNPshot | rs34028295 |
| SNPdbe | rs34028295 |
| MSV3d | rs34028295 |
| GWAS Ctlg | rs34028295 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs34028295(G;G) |
| Alt | rs34028295(G;G) |
| Reference | Rs34028295(-;-) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | COX14 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000012.11:g.50513907dupG |
| CLNSRC | |
| CLNACC | RCV000196387.1, |
