rs748468371
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (CT;CT) | 0 | common in clinvar |
| Make rs748468371(-;-) |
| Make rs748468371(-;CT) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 10 |
| Position | 99727554 |
| Gene | COX15 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs748468371 |
| dbSNP (classic) | rs748468371 |
| ClinGen | rs748468371 |
| ebi | rs748468371 |
| HLI | rs748468371 |
| Exac | rs748468371 |
| Gnomad | rs748468371 |
| Varsome | rs748468371 |
| LitVar | rs748468371 |
| Map | rs748468371 |
| PheGenI | rs748468371 |
| Biobank | rs748468371 |
| 1000 genomes | rs748468371 |
| hgdp | rs748468371 |
| ensembl | rs748468371 |
| geneview | rs748468371 |
| scholar | rs748468371 |
| rs748468371 | |
| pharmgkb | rs748468371 |
| gwascentral | rs748468371 |
| openSNP | rs748468371 |
| 23andMe | rs748468371 |
| SNPshot | rs748468371 |
| SNPdbe | rs748468371 |
| MSV3d | rs748468371 |
| GWAS Ctlg | rs748468371 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs748468371(-;-) |
| Alt | rs748468371(-;-) |
| Reference | Rs748468371(CT;CT) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | COX15 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000010.10:g.101487311_101487312delCT |
| CLNSRC | |
| CLNACC | RCV000493741.1, |
