rs72657692
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs72657692(C;C) |
| Make rs72657692(C;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 16169667 |
| Gene | ABCC6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs72657692 |
| dbSNP (classic) | rs72657692 |
| ClinGen | rs72657692 |
| ebi | rs72657692 |
| HLI | rs72657692 |
| Exac | rs72657692 |
| Gnomad | rs72657692 |
| Varsome | rs72657692 |
| LitVar | rs72657692 |
| Map | rs72657692 |
| PheGenI | rs72657692 |
| Biobank | rs72657692 |
| 1000 genomes | rs72657692 |
| hgdp | rs72657692 |
| ensembl | rs72657692 |
| geneview | rs72657692 |
| scholar | rs72657692 |
| rs72657692 | |
| pharmgkb | rs72657692 |
| gwascentral | rs72657692 |
| openSNP | rs72657692 |
| 23andMe | rs72657692 |
| SNPshot | rs72657692 |
| SNPdbe | rs72657692 |
| MSV3d | rs72657692 |
| GWAS Ctlg | rs72657692 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs72657692(C;C) |
| Alt | rs72657692(C;C) |
| Reference | Rs72657692(G;G) |
| Significance | Untested |
| Disease | |
| Variation | info |
| Gene | ABCC6 |
| CLNDBN | |
| Reversed | 1 |
| HGVS | NC_000016.9:g.16263524C>G |
| CLNSRC | |
| CLNACC | |
