rs67791546
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs67791546(-;-) |
| Make rs67791546(-;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 16154654 |
| Gene | ABCC6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs67791546 |
| dbSNP (classic) | rs67791546 |
| ClinGen | rs67791546 |
| ebi | rs67791546 |
| HLI | rs67791546 |
| Exac | rs67791546 |
| Gnomad | rs67791546 |
| Varsome | rs67791546 |
| LitVar | rs67791546 |
| Map | rs67791546 |
| PheGenI | rs67791546 |
| Biobank | rs67791546 |
| 1000 genomes | rs67791546 |
| hgdp | rs67791546 |
| ensembl | rs67791546 |
| geneview | rs67791546 |
| scholar | rs67791546 |
| rs67791546 | |
| pharmgkb | rs67791546 |
| gwascentral | rs67791546 |
| openSNP | rs67791546 |
| 23andMe | rs67791546 |
| SNPshot | rs67791546 |
| SNPdbe | rs67791546 |
| MSV3d | rs67791546 |
| GWAS Ctlg | rs67791546 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | |
| Alt | |
| Reference | Rs67791546(G;G) |
| Significance | Untested |
| Disease | |
| Variation | info |
| Gene | ABCC6 |
| CLNDBN | |
| Reversed | 1 |
| HGVS | NC_000016.9:g.16248511delC |
| CLNSRC | |
| CLNACC | |
[PMID 12673275] ABCC6/MRP6 mutations: further insight into the molecular pathology of pseudoxanthoma elasticum.
