rs66616070
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs66616070(A;A) |
| Make rs66616070(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 16182414 |
| Gene | ABCC6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs66616070 |
| dbSNP (classic) | rs66616070 |
| ClinGen | rs66616070 |
| ebi | rs66616070 |
| HLI | rs66616070 |
| Exac | rs66616070 |
| Gnomad | rs66616070 |
| Varsome | rs66616070 |
| LitVar | rs66616070 |
| Map | rs66616070 |
| PheGenI | rs66616070 |
| Biobank | rs66616070 |
| 1000 genomes | rs66616070 |
| hgdp | rs66616070 |
| ensembl | rs66616070 |
| geneview | rs66616070 |
| scholar | rs66616070 |
| rs66616070 | |
| pharmgkb | rs66616070 |
| gwascentral | rs66616070 |
| openSNP | rs66616070 |
| 23andMe | rs66616070 |
| SNPshot | rs66616070 |
| SNPdbe | rs66616070 |
| MSV3d | rs66616070 |
| GWAS Ctlg | rs66616070 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs66616070(A;A) |
| Alt | rs66616070(A;A) |
| Reference | Rs66616070(G;G) |
| Significance | Untested |
| Disease | |
| Variation | info |
| Gene | ABCC6 |
| CLNDBN | |
| Reversed | 0 |
| HGVS | NC_000016.9:g.16276271G>A |
| CLNSRC | |
| CLNACC | |
