rs6020
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs6020(A;A) |
| Make rs6020(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 169549874 |
| Gene | F5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6020 |
| dbSNP (classic) | rs6020 |
| ClinGen | rs6020 |
| ebi | rs6020 |
| HLI | rs6020 |
| Exac | rs6020 |
| Gnomad | rs6020 |
| Varsome | rs6020 |
| LitVar | rs6020 |
| Map | rs6020 |
| PheGenI | rs6020 |
| Biobank | rs6020 |
| 1000 genomes | rs6020 |
| hgdp | rs6020 |
| ensembl | rs6020 |
| geneview | rs6020 |
| scholar | rs6020 |
| rs6020 | |
| pharmgkb | rs6020 |
| gwascentral | rs6020 |
| openSNP | rs6020 |
| 23andMe | rs6020 |
| SNPshot | rs6020 |
| SNPdbe | rs6020 |
| MSV3d | rs6020 |
| GWAS Ctlg | rs6020 |
| GMAF | 0.2649 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 23954867] The association of idiopathic recurrent pregnancy loss with polymorphisms in haemostasis-related genes
[PMID 18974781
] Cataloging coding sequence variations in human genome databases.
[PMID 25119470] Single Nucleotide Polymorphisms Other than Factor V Leiden Are Associated with Coagulopathy and Osteonecrosis of the Femoral Head in Chinese Patients
| ClinVar | |
|---|---|
| Risk | rs6020(A;A) |
| Alt | rs6020(A;A) |
| Reference | Rs6020(G;G) |
| Significance | Probable-non-pathogenic |
| Disease | Thrombophilia due to activated protein C resistance |
| Variation | info |
| Gene | F5 |
| CLNDBN | Thrombophilia due to activated protein C resistance |
| Reversed | 1 |
| HGVS | NC_000001.10:g.169519112C>T |
| CLNSRC | |
| CLNACC | RCV000333894.1, |
