rs1044291
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs1044291(C;T) |
| Make rs1044291(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 154572200 |
| Gene | FGB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1044291 |
| dbSNP (classic) | rs1044291 |
| ClinGen | rs1044291 |
| ebi | rs1044291 |
| HLI | rs1044291 |
| Exac | rs1044291 |
| Gnomad | rs1044291 |
| Varsome | rs1044291 |
| LitVar | rs1044291 |
| Map | rs1044291 |
| PheGenI | rs1044291 |
| Biobank | rs1044291 |
| 1000 genomes | rs1044291 |
| hgdp | rs1044291 |
| ensembl | rs1044291 |
| geneview | rs1044291 |
| scholar | rs1044291 |
| rs1044291 | |
| pharmgkb | rs1044291 |
| gwascentral | rs1044291 |
| openSNP | rs1044291 |
| 23andMe | rs1044291 |
| SNPshot | rs1044291 |
| SNPdbe | rs1044291 |
| MSV3d | rs1044291 |
| GWAS Ctlg | rs1044291 |
| GMAF | 0.1993 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20135074] A genetic variant in the gene encoding fibrinogen beta chain predicted development of hypertension in Chinese men
[PMID 18974842
] Gender differences in genetic risk profiles for cardiovascular disease.
[PMID 20031577] Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study.
| ClinVar | |
|---|---|
| Risk | rs1044291(T;T) |
| Alt | rs1044291(T;T) |
| Reference | Rs1044291(C;C) |
| Significance | Non-pathogenic |
| Disease | Afibrinogenemia |
| Variation | info |
| Gene | FGB |
| CLNDBN | Afibrinogenemia, congenital |
| Reversed | 0 |
| HGVS | NC_000004.11:g.155493352C>T |
| CLNSRC | |
| CLNACC | RCV000314054.1, |
