rs2292350
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2292350(A;A) |
| Make rs2292350(A;G) |
| Make rs2292350(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 6998353 |
| Gene | ALOX12, ALOX12-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2292350 |
| dbSNP (classic) | rs2292350 |
| ClinGen | rs2292350 |
| ebi | rs2292350 |
| HLI | rs2292350 |
| Exac | rs2292350 |
| Gnomad | rs2292350 |
| Varsome | rs2292350 |
| LitVar | rs2292350 |
| Map | rs2292350 |
| PheGenI | rs2292350 |
| Biobank | rs2292350 |
| 1000 genomes | rs2292350 |
| hgdp | rs2292350 |
| ensembl | rs2292350 |
| geneview | rs2292350 |
| scholar | rs2292350 |
| rs2292350 | |
| pharmgkb | rs2292350 |
| gwascentral | rs2292350 |
| openSNP | rs2292350 |
| 23andMe | rs2292350 |
| SNPshot | rs2292350 |
| SNPdbe | rs2292350 |
| MSV3d | rs2292350 |
| GWAS Ctlg | rs2292350 |
| GMAF | 0.3145 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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| ||
[PMID 21104233] Polymorphisms in the ALOX12 gene and osteoporosis
[PMID 18640486
] Association of arachidonate 12-lipoxygenase genotype variation and glycemic control with albuminuria in type 2 diabetes.
[PMID 19774229] The relationship of DNA methylation with age, gender and genotype in twins and healthy controls.
[PMID 20592751] Human lipoxygenase pathway gene variation and association with markers of subclinical atherosclerosis in the diabetes heart study.
[PMID 22668814] Association of ALOX12 and ALOX15 gene polymorphisms with age at menarche and natural menopause in Chinese women.
[PMID 30277667] ALOX12 gene polymorphisms and serum selenium status in elderly osteoporotic patients.
