rs145068530
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs145068530(A;G) |
| Make rs145068530(G;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 5 |
| Position | 132384178 |
| Gene | SLC22A5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs145068530 |
| dbSNP (classic) | rs145068530 |
| ClinGen | rs145068530 |
| ebi | rs145068530 |
| HLI | rs145068530 |
| Exac | rs145068530 |
| Gnomad | rs145068530 |
| Varsome | rs145068530 |
| LitVar | rs145068530 |
| Map | rs145068530 |
| PheGenI | rs145068530 |
| Biobank | rs145068530 |
| 1000 genomes | rs145068530 |
| hgdp | rs145068530 |
| ensembl | rs145068530 |
| geneview | rs145068530 |
| scholar | rs145068530 |
| rs145068530 | |
| pharmgkb | rs145068530 |
| gwascentral | rs145068530 |
| openSNP | rs145068530 |
| 23andMe | rs145068530 |
| SNPshot | rs145068530 |
| SNPdbe | rs145068530 |
| MSV3d | rs145068530 |
| GWAS Ctlg | rs145068530 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs145068530(G;G) |
| Alt | rs145068530(G;G) |
| Reference | Rs145068530(A;A) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | SLC22A5 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000005.9:g.131719870A>G |
| CLNSRC | |
| CLNACC | RCV000434160.1, |
