rs533335580
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| (C;T) | 3 | carrier of factor XI mutation |
| (T;T) | 5 | Factor XI deficiency |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 4 |
| Position | 186284155 |
| Gene | F11 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs533335580 |
| dbSNP (classic) | rs533335580 |
| ClinGen | rs533335580 |
| ebi | rs533335580 |
| HLI | rs533335580 |
| Exac | rs533335580 |
| Gnomad | rs533335580 |
| Varsome | rs533335580 |
| LitVar | rs533335580 |
| Map | rs533335580 |
| PheGenI | rs533335580 |
| Biobank | rs533335580 |
| 1000 genomes | rs533335580 |
| hgdp | rs533335580 |
| ensembl | rs533335580 |
| geneview | rs533335580 |
| scholar | rs533335580 |
| rs533335580 | |
| pharmgkb | rs533335580 |
| gwascentral | rs533335580 |
| openSNP | rs533335580 |
| 23andMe | rs533335580 |
| SNPshot | rs533335580 |
| SNPdbe | rs533335580 |
| MSV3d | rs533335580 |
| GWAS Ctlg | rs533335580 |
| Max Magnitude | 5 |
| ClinVar | |
|---|---|
| Risk | Rs533335580(T;T) |
| Alt | Rs533335580(T;T) |
| Reference | Rs533335580(C;C) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | F11 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000004.11:g.187205309C>T |
| CLNSRC | |
| CLNACC | RCV000428449.1, |
