rs57499803
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs57499803(C;T) |
| Make rs57499803(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 16154936 |
| Gene | ABCC6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs57499803 |
| dbSNP (classic) | rs57499803 |
| ClinGen | rs57499803 |
| ebi | rs57499803 |
| HLI | rs57499803 |
| Exac | rs57499803 |
| Gnomad | rs57499803 |
| Varsome | rs57499803 |
| LitVar | rs57499803 |
| Map | rs57499803 |
| PheGenI | rs57499803 |
| Biobank | rs57499803 |
| 1000 genomes | rs57499803 |
| hgdp | rs57499803 |
| ensembl | rs57499803 |
| geneview | rs57499803 |
| scholar | rs57499803 |
| rs57499803 | |
| pharmgkb | rs57499803 |
| gwascentral | rs57499803 |
| openSNP | rs57499803 |
| 23andMe | rs57499803 |
| SNPshot | rs57499803 |
| SNPdbe | rs57499803 |
| MSV3d | rs57499803 |
| GWAS Ctlg | rs57499803 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs57499803(T;T) |
| Alt | rs57499803(T;T) |
| Reference | Rs57499803(C;C) |
| Significance | Untested |
| Disease | |
| Variation | info |
| Gene | ABCC6 |
| CLNDBN | |
| Reversed | 1 |
| HGVS | NC_000016.9:g.16248793G>A |
| CLNSRC | |
| CLNACC | |
