rs367891946
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs367891946(C;G) |
| Make rs367891946(G;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 15 |
| Position | 40418127 |
| Gene | IVD |
| is a | snp |
| is | mentioned by |
| dbSNP | rs367891946 |
| dbSNP (classic) | rs367891946 |
| ClinGen | rs367891946 |
| ebi | rs367891946 |
| HLI | rs367891946 |
| Exac | rs367891946 |
| Gnomad | rs367891946 |
| Varsome | rs367891946 |
| LitVar | rs367891946 |
| Map | rs367891946 |
| PheGenI | rs367891946 |
| Biobank | rs367891946 |
| 1000 genomes | rs367891946 |
| hgdp | rs367891946 |
| ensembl | rs367891946 |
| geneview | rs367891946 |
| scholar | rs367891946 |
| rs367891946 | |
| pharmgkb | rs367891946 |
| gwascentral | rs367891946 |
| openSNP | rs367891946 |
| 23andMe | rs367891946 |
| SNPshot | rs367891946 |
| SNPdbe | rs367891946 |
| MSV3d | rs367891946 |
| GWAS Ctlg | rs367891946 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs367891946(G;G) |
| Alt | rs367891946(G;G) |
| Reference | Rs367891946(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | IVD |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000015.9:g.40710326C>G |
| CLNSRC | |
| CLNACC | RCV000185977.1, |
