rs4765127
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4765127(G;G) |
| Make rs4765127(G;T) |
| Make rs4765127(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 123975620 |
| Gene | ZNF664, ZNF664-FAM101A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4765127 |
| dbSNP (classic) | rs4765127 |
| ClinGen | rs4765127 |
| ebi | rs4765127 |
| HLI | rs4765127 |
| Exac | rs4765127 |
| Gnomad | rs4765127 |
| Varsome | rs4765127 |
| LitVar | rs4765127 |
| Map | rs4765127 |
| PheGenI | rs4765127 |
| Biobank | rs4765127 |
| 1000 genomes | rs4765127 |
| hgdp | rs4765127 |
| ensembl | rs4765127 |
| geneview | rs4765127 |
| scholar | rs4765127 |
| rs4765127 | |
| pharmgkb | rs4765127 |
| gwascentral | rs4765127 |
| openSNP | rs4765127 |
| 23andMe | rs4765127 |
| SNPshot | rs4765127 |
| SNPdbe | rs4765127 |
| MSV3d | rs4765127 |
| GWAS Ctlg | rs4765127 |
| GMAF | 0.2842 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20686565 ]
|
| Trait | |
| Title | Biological, clinical and population relevance of 95 loci for blood lipids. |
| Risk Allele | G |
| P-val | 1E-8 |
| Odds Ratio | 2.4200 None |
| GWAS snp | |
|---|---|
| PMID | [PMID 24097068]
|
| Trait | HDL cholesterol |
| Title | Discovery and refinement of loci associated with lipid levels. |
| Risk Allele | T |
| P-val | 8E-10 |
| Odds Ratio | .03 [NR] unit increase |
[PMID 30275878] Direct and indirect genetic effects on triglycerides through omics and correlated phenotypes.
