rs201079485
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs201079485(A;A) |
| Make rs201079485(A;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 11 |
| Position | 116790940 |
| Gene | APOA5, ZPR1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs201079485 |
| dbSNP (classic) | rs201079485 |
| ClinGen | rs201079485 |
| ebi | rs201079485 |
| HLI | rs201079485 |
| Exac | rs201079485 |
| Gnomad | rs201079485 |
| Varsome | rs201079485 |
| LitVar | rs201079485 |
| Map | rs201079485 |
| PheGenI | rs201079485 |
| Biobank | rs201079485 |
| 1000 genomes | rs201079485 |
| hgdp | rs201079485 |
| ensembl | rs201079485 |
| geneview | rs201079485 |
| scholar | rs201079485 |
| rs201079485 | |
| pharmgkb | rs201079485 |
| gwascentral | rs201079485 |
| openSNP | rs201079485 |
| 23andMe | rs201079485 |
| SNPshot | rs201079485 |
| SNPdbe | rs201079485 |
| MSV3d | rs201079485 |
| GWAS Ctlg | rs201079485 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs201079485(A;A) rs201079485(T;T) |
| Alt | rs201079485(A;A) rs201079485(T;T) |
| Reference | Rs201079485(G;G) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | APOA5 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000011.9:g.116661656G>A |
| CLNSRC | |
| CLNACC | RCV000428946.1, |
