rs59002125
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs59002125(C;T) |
| Make rs59002125(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 16 |
| Position | 16182884 |
| Gene | ABCC6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs59002125 |
| dbSNP (classic) | rs59002125 |
| ClinGen | rs59002125 |
| ebi | rs59002125 |
| HLI | rs59002125 |
| Exac | rs59002125 |
| Gnomad | rs59002125 |
| Varsome | rs59002125 |
| LitVar | rs59002125 |
| Map | rs59002125 |
| PheGenI | rs59002125 |
| Biobank | rs59002125 |
| 1000 genomes | rs59002125 |
| hgdp | rs59002125 |
| ensembl | rs59002125 |
| geneview | rs59002125 |
| scholar | rs59002125 |
| rs59002125 | |
| pharmgkb | rs59002125 |
| gwascentral | rs59002125 |
| openSNP | rs59002125 |
| 23andMe | rs59002125 |
| SNPshot | rs59002125 |
| SNPdbe | rs59002125 |
| MSV3d | rs59002125 |
| GWAS Ctlg | rs59002125 |
| GMAF | 0.001377 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs59002125(T;T) |
| Alt | rs59002125(T;T) |
| Reference | Rs59002125(C;C) |
| Significance | Untested |
| Disease | |
| Variation | info |
| Gene | ABCC6 |
| CLNDBN | |
| Reversed | 1 |
| HGVS | NC_000016.9:g.16276741G>A |
| CLNSRC | |
| CLNACC | |
[PMID 16127278] Analysis of sequence variations in the ABCC6 gene among patients with abdominal aortic aneurysm and pseudoxanthoma elasticum.
