rs397517184
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs397517184(C;C) |
| Make rs397517184(C;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 12 |
| Position | 21906141 |
| Gene | ABCC9 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs397517184 |
| dbSNP (classic) | rs397517184 |
| ClinGen | rs397517184 |
| ebi | rs397517184 |
| HLI | rs397517184 |
| Exac | rs397517184 |
| Gnomad | rs397517184 |
| Varsome | rs397517184 |
| LitVar | rs397517184 |
| Map | rs397517184 |
| PheGenI | rs397517184 |
| Biobank | rs397517184 |
| 1000 genomes | rs397517184 |
| hgdp | rs397517184 |
| ensembl | rs397517184 |
| geneview | rs397517184 |
| scholar | rs397517184 |
| rs397517184 | |
| pharmgkb | rs397517184 |
| gwascentral | rs397517184 |
| openSNP | rs397517184 |
| 23andMe | rs397517184 |
| SNPshot | rs397517184 |
| SNPdbe | rs397517184 |
| MSV3d | rs397517184 |
| GWAS Ctlg | rs397517184 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs397517184(C;C) |
| Alt | rs397517184(C;C) |
| Reference | Rs397517184(T;T) |
| Significance | Other |
| Disease | not specified |
| Variation | info |
| Gene | ABCC9 |
| CLNDBN | not specified |
| Reversed | 1 |
| HGVS | NC_000012.11:g.22059075A>G |
| CLNSRC | |
| CLNACC | RCV000038586.4, |
