rs146457619
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs146457619(A;G) |
| Make rs146457619(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 7 |
| Position | 143339304 |
| Gene | CLCN1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs146457619 |
| dbSNP (classic) | rs146457619 |
| ClinGen | rs146457619 |
| ebi | rs146457619 |
| HLI | rs146457619 |
| Exac | rs146457619 |
| Gnomad | rs146457619 |
| Varsome | rs146457619 |
| LitVar | rs146457619 |
| Map | rs146457619 |
| PheGenI | rs146457619 |
| Biobank | rs146457619 |
| 1000 genomes | rs146457619 |
| hgdp | rs146457619 |
| ensembl | rs146457619 |
| geneview | rs146457619 |
| scholar | rs146457619 |
| rs146457619 | |
| pharmgkb | rs146457619 |
| gwascentral | rs146457619 |
| openSNP | rs146457619 |
| 23andMe | rs146457619 |
| SNPshot | rs146457619 |
| SNPdbe | rs146457619 |
| MSV3d | rs146457619 |
| GWAS Ctlg | rs146457619 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs146457619(G;G) |
| Alt | rs146457619(G;G) |
| Reference | Rs146457619(A;A) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | CLCN1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000007.13:g.143036397A>G |
| CLNSRC | |
| CLNACC | RCV000342021.1, |
