rs565513365
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs565513365(A;G) |
| Make rs565513365(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 1 |
| Position | 11966985 |
| Gene | PLOD1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs565513365 |
| dbSNP (classic) | rs565513365 |
| ClinGen | rs565513365 |
| ebi | rs565513365 |
| HLI | rs565513365 |
| Exac | rs565513365 |
| Gnomad | rs565513365 |
| Varsome | rs565513365 |
| LitVar | rs565513365 |
| Map | rs565513365 |
| PheGenI | rs565513365 |
| Biobank | rs565513365 |
| 1000 genomes | rs565513365 |
| hgdp | rs565513365 |
| ensembl | rs565513365 |
| geneview | rs565513365 |
| scholar | rs565513365 |
| rs565513365 | |
| pharmgkb | rs565513365 |
| gwascentral | rs565513365 |
| openSNP | rs565513365 |
| 23andMe | rs565513365 |
| SNPshot | rs565513365 |
| SNPdbe | rs565513365 |
| MSV3d | rs565513365 |
| GWAS Ctlg | rs565513365 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs565513365(G;G) |
| Alt | rs565513365(G;G) |
| Reference | Rs565513365(A;A) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | PLOD1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000001.10:g.12027042A>G |
| CLNSRC | |
| CLNACC | RCV000254922.1, |
