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.
