rs188698686
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs188698686(A;G) |
| Make rs188698686(G;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 5 |
| Position | 132385369 |
| Gene | SLC22A5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs188698686 |
| dbSNP (classic) | rs188698686 |
| ClinGen | rs188698686 |
| ebi | rs188698686 |
| HLI | rs188698686 |
| Exac | rs188698686 |
| Gnomad | rs188698686 |
| Varsome | rs188698686 |
| LitVar | rs188698686 |
| Map | rs188698686 |
| PheGenI | rs188698686 |
| Biobank | rs188698686 |
| 1000 genomes | rs188698686 |
| hgdp | rs188698686 |
| ensembl | rs188698686 |
| geneview | rs188698686 |
| scholar | rs188698686 |
| rs188698686 | |
| pharmgkb | rs188698686 |
| gwascentral | rs188698686 |
| openSNP | rs188698686 |
| 23andMe | rs188698686 |
| SNPshot | rs188698686 |
| SNPdbe | rs188698686 |
| MSV3d | rs188698686 |
| GWAS Ctlg | rs188698686 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs188698686(G;G) |
| Alt | rs188698686(G;G) |
| Reference | Rs188698686(A;A) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | SLC22A5 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000005.9:g.131721061A>C |
| CLNSRC | |
| CLNACC | RCV000186138.1, |
