rs61753266
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs61753266(A;A) |
| Make rs61753266(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 113140972 |
| Gene | F10 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs61753266 |
| dbSNP (classic) | rs61753266 |
| ClinGen | rs61753266 |
| ebi | rs61753266 |
| HLI | rs61753266 |
| Exac | rs61753266 |
| Gnomad | rs61753266 |
| Varsome | rs61753266 |
| LitVar | rs61753266 |
| Map | rs61753266 |
| PheGenI | rs61753266 |
| Biobank | rs61753266 |
| 1000 genomes | rs61753266 |
| hgdp | rs61753266 |
| ensembl | rs61753266 |
| geneview | rs61753266 |
| scholar | rs61753266 |
| rs61753266 | |
| pharmgkb | rs61753266 |
| gwascentral | rs61753266 |
| openSNP | rs61753266 |
| 23andMe | rs61753266 |
| SNPshot | rs61753266 |
| SNPdbe | rs61753266 |
| MSV3d | rs61753266 |
| GWAS Ctlg | rs61753266 |
| GMAF | 0.0009183 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs61753266(A;A) |
| Alt | rs61753266(A;A) |
| Reference | Rs61753266(G;G) |
| Significance | Pathogenic |
| Disease | Factor X deficiency |
| Variation | info |
| Gene | F10 |
| CLNDBN | Factor X deficiency |
| Reversed | 0 |
| HGVS | NC_000013.10:g.113795286G>A |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000012841.4, |
