rs1748195
| Orientation | plus |
| Stabilized | plus |
| Make rs1748195(C;C) |
| Make rs1748195(C;G) |
| Make rs1748195(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 62583922 |
| Gene | DOCK7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1748195 |
| dbSNP (classic) | rs1748195 |
| ClinGen | rs1748195 |
| ebi | rs1748195 |
| HLI | rs1748195 |
| Exac | rs1748195 |
| Gnomad | rs1748195 |
| Varsome | rs1748195 |
| LitVar | rs1748195 |
| Map | rs1748195 |
| PheGenI | rs1748195 |
| Biobank | rs1748195 |
| 1000 genomes | rs1748195 |
| hgdp | rs1748195 |
| ensembl | rs1748195 |
| geneview | rs1748195 |
| scholar | rs1748195 |
| rs1748195 | |
| pharmgkb | rs1748195 |
| gwascentral | rs1748195 |
| openSNP | rs1748195 |
| 23andMe | rs1748195 |
| SNPshot | rs1748195 |
| SNPdbe | rs1748195 |
| MSV3d | rs1748195 |
| GWAS Ctlg | rs1748195 |
| GMAF | 0.3792 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS | |
|---|---|
| SNP | rs1748195 |
| PubMedID | [PMID 18193043 ]
|
| Condition | Triglycerides |
| Gene | ANGPTL3 |
| Risk Allele | C |
| pValue | 2.00E-010 |
| OR | 7.12 |
| 95% CI | NR) mg/dl highe |
[PMID 18852197] Metabolic and cardiovascular traits: an abundance of recently identified common genetic variants.
[PMID 19060910] Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.
[PMID 19185284] Common variation in the beta-carotene 15,15'-monooxygenase 1 gene affects circulating levels of carotenoids: a genome-wide association study.
[PMID 19299407] Replication of genetic associations with plasma lipoprotein traits in a multiethnic sample.
[PMID 19435741] Common lipid-altering gene variants are associated with therapeutic intervention thresholds of lipid levels in older people.
[PMID 19656773] A polygenic basis for four classical Fredrickson hyperlipoproteinemia phenotypes that are characterized by hypertriglyceridemia.
[PMID 20369022] Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.
[PMID 23832694] Common genetic variants associated with lipid profiles in a Chinese pediatric population.
[PMID 29454388] DOCK7-ANGPTL3 SNPs and their haplotypes with serum lipid levels and the risk of coronary artery disease and ischemic stroke.
