rs966681982
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 17 |
| Position | 6703140 |
| Gene | SLC13A5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs966681982 |
| dbSNP (classic) | rs966681982 |
| ClinGen | rs966681982 |
| ebi | rs966681982 |
| HLI | rs966681982 |
| Exac | rs966681982 |
| Gnomad | rs966681982 |
| Varsome | rs966681982 |
| LitVar | rs966681982 |
| Map | rs966681982 |
| PheGenI | rs966681982 |
| Biobank | rs966681982 |
| 1000 genomes | rs966681982 |
| hgdp | rs966681982 |
| ensembl | rs966681982 |
| geneview | rs966681982 |
| scholar | rs966681982 |
| rs966681982 | |
| pharmgkb | rs966681982 |
| gwascentral | rs966681982 |
| openSNP | rs966681982 |
| 23andMe | rs966681982 |
| SNPshot | rs966681982 |
| SNPdbe | rs966681982 |
| MSV3d | rs966681982 |
| GWAS Ctlg | rs966681982 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs966681982(C;C) |
| Alt | rs966681982(C;C) |
| Reference | Rs966681982(T;T) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000017.10:g.6606459T>C |
| CLNSRC | |
| CLNACC | RCV000485335.1, |
