rs142553916
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs142553916(A;A) |
| Make rs142553916(A;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 6 |
| Position | 73621883 |
| Gene | SLC17A5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs142553916 |
| dbSNP (classic) | rs142553916 |
| ClinGen | rs142553916 |
| ebi | rs142553916 |
| HLI | rs142553916 |
| Exac | rs142553916 |
| Gnomad | rs142553916 |
| Varsome | rs142553916 |
| LitVar | rs142553916 |
| Map | rs142553916 |
| PheGenI | rs142553916 |
| Biobank | rs142553916 |
| 1000 genomes | rs142553916 |
| hgdp | rs142553916 |
| ensembl | rs142553916 |
| geneview | rs142553916 |
| scholar | rs142553916 |
| rs142553916 | |
| pharmgkb | rs142553916 |
| gwascentral | rs142553916 |
| openSNP | rs142553916 |
| 23andMe | rs142553916 |
| SNPshot | rs142553916 |
| SNPdbe | rs142553916 |
| MSV3d | rs142553916 |
| GWAS Ctlg | rs142553916 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs142553916(A;A) |
| Alt | rs142553916(A;A) |
| Reference | Rs142553916(G;G) |
| Significance | Other |
| Disease | not provided |
| Variation | info |
| Gene | SLC17A5 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000006.11:g.74331606G>A |
| CLNSRC | |
| CLNACC | RCV000171400.2, |
