rs2267439
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2267439(C;C) |
| Make rs2267439(C;T) |
| Make rs2267439(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 41841765 |
| Gene | SREBF2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2267439 |
| dbSNP (classic) | rs2267439 |
| ClinGen | rs2267439 |
| ebi | rs2267439 |
| HLI | rs2267439 |
| Exac | rs2267439 |
| Gnomad | rs2267439 |
| Varsome | rs2267439 |
| LitVar | rs2267439 |
| Map | rs2267439 |
| PheGenI | rs2267439 |
| Biobank | rs2267439 |
| 1000 genomes | rs2267439 |
| hgdp | rs2267439 |
| ensembl | rs2267439 |
| geneview | rs2267439 |
| scholar | rs2267439 |
| rs2267439 | |
| pharmgkb | rs2267439 |
| gwascentral | rs2267439 |
| openSNP | rs2267439 |
| 23andMe | rs2267439 |
| SNPshot | rs2267439 |
| SNPdbe | rs2267439 |
| MSV3d | rs2267439 |
| GWAS Ctlg | rs2267439 |
| GMAF | 0.2897 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 18954446
] avascular necrosis (AVN), a bone disease that produces osteonecrosis of the femoral head. The minor allele (C) frequency of rs2267439 showed a significant protective effect, while rs1052717 and rs2267443 were significantly associated with AVN risk
[PMID 31490983] SREBF1c and SREBF2 gene polymorphisms are associated with acute coronary syndrome and blood lipid levels in Mexican population.
