rs2070852
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs2070852(C;C) |
| Make rs2070852(C;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 46723375 |
| Gene | F2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2070852 |
| dbSNP (classic) | rs2070852 |
| ClinGen | rs2070852 |
| ebi | rs2070852 |
| HLI | rs2070852 |
| Exac | rs2070852 |
| Gnomad | rs2070852 |
| Varsome | rs2070852 |
| LitVar | rs2070852 |
| Map | rs2070852 |
| PheGenI | rs2070852 |
| Biobank | rs2070852 |
| 1000 genomes | rs2070852 |
| hgdp | rs2070852 |
| ensembl | rs2070852 |
| geneview | rs2070852 |
| scholar | rs2070852 |
| rs2070852 | |
| pharmgkb | rs2070852 |
| gwascentral | rs2070852 |
| openSNP | rs2070852 |
| 23andMe | rs2070852 |
| SNPshot | rs2070852 |
| SNPdbe | rs2070852 |
| MSV3d | rs2070852 |
| GWAS Ctlg | rs2070852 |
| GMAF | 0.4481 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 24162564] Association between prothrombin gene polymorphisms and hereditary thrombophilia in Xinjiang Kazakhs population
[PMID 19369658
] Genomewide association studies of stroke.
[PMID 19801982] Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.
[PMID 19841454] Collaborative meta-analysis: associations of 150 candidate genes with osteoporosis and osteoporotic fracture.
| ClinVar | |
|---|---|
| Risk | rs2070852(C;C) |
| Alt | rs2070852(C;C) |
| Reference | Rs2070852(G;G) |
| Significance | Probable-non-pathogenic |
| Disease | not specified Thrombophilia Hereditary factor II deficiency disease |
| Variation | info |
| Gene | F2 |
| CLNDBN | not specified Thrombophilia Hereditary factor II deficiency disease |
| Reversed | 0 |
| HGVS | NC_000011.9:g.46744925G>C |
| CLNSRC | |
| CLNACC | RCV000246968.1, RCV000340341.1, RCV000396449.1, |
