rs72653792
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs72653792(G;T) |
| Make rs72653792(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 16 |
| Position | 16178854 |
| Gene | ABCC6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs72653792 |
| dbSNP (classic) | rs72653792 |
| ClinGen | rs72653792 |
| ebi | rs72653792 |
| HLI | rs72653792 |
| Exac | rs72653792 |
| Gnomad | rs72653792 |
| Varsome | rs72653792 |
| LitVar | rs72653792 |
| Map | rs72653792 |
| PheGenI | rs72653792 |
| Biobank | rs72653792 |
| 1000 genomes | rs72653792 |
| hgdp | rs72653792 |
| ensembl | rs72653792 |
| geneview | rs72653792 |
| scholar | rs72653792 |
| rs72653792 | |
| pharmgkb | rs72653792 |
| gwascentral | rs72653792 |
| openSNP | rs72653792 |
| 23andMe | rs72653792 |
| SNPshot | rs72653792 |
| SNPdbe | rs72653792 |
| MSV3d | rs72653792 |
| GWAS Ctlg | rs72653792 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs72653792(A;A) rs72653792(T;T) |
| Alt | rs72653792(A;A) rs72653792(T;T) |
| Reference | Rs72653792(G;G) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | ABCC6 |
| CLNDBN | not provided |
| Reversed | 1 |
| HGVS | NC_000016.9:g.16272711C>T |
| CLNSRC | |
| CLNACC | RCV000483030.1, |
