rs5962
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs5962(C;T) |
| Make rs5962(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 113140947 |
| Gene | F10 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5962 |
| dbSNP (classic) | rs5962 |
| ClinGen | rs5962 |
| ebi | rs5962 |
| HLI | rs5962 |
| Exac | rs5962 |
| Gnomad | rs5962 |
| Varsome | rs5962 |
| LitVar | rs5962 |
| Map | rs5962 |
| PheGenI | rs5962 |
| Biobank | rs5962 |
| 1000 genomes | rs5962 |
| hgdp | rs5962 |
| ensembl | rs5962 |
| geneview | rs5962 |
| scholar | rs5962 |
| rs5962 | |
| pharmgkb | rs5962 |
| gwascentral | rs5962 |
| openSNP | rs5962 |
| 23andMe | rs5962 |
| SNPshot | rs5962 |
| SNPdbe | rs5962 |
| MSV3d | rs5962 |
| GWAS Ctlg | rs5962 |
| GMAF | 0.02296 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19724895] Association of gene polymorphisms with chronic kidney disease in Japanese individuals
| ClinVar | |
|---|---|
| Risk | rs5962(T;T) |
| Alt | rs5962(T;T) |
| Reference | Rs5962(C;C) |
| Significance | Probable-non-pathogenic |
| Disease | Factor X deficiency |
| Variation | info |
| Gene | F10 |
| CLNDBN | Factor X deficiency |
| Reversed | 0 |
| HGVS | NC_000013.10:g.113795261C>T |
| CLNSRC | |
| CLNACC | RCV000270472.1, |
