rs10490626
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 |
| Make rs10490626(C;T) |
| Make rs10490626(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 118078265 |
| Gene | LOC107985940 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10490626 |
| dbSNP (classic) | rs10490626 |
| ClinGen | rs10490626 |
| ebi | rs10490626 |
| HLI | rs10490626 |
| Exac | rs10490626 |
| Gnomad | rs10490626 |
| Varsome | rs10490626 |
| LitVar | rs10490626 |
| Map | rs10490626 |
| PheGenI | rs10490626 |
| Biobank | rs10490626 |
| 1000 genomes | rs10490626 |
| hgdp | rs10490626 |
| ensembl | rs10490626 |
| geneview | rs10490626 |
| scholar | rs10490626 |
| rs10490626 | |
| pharmgkb | rs10490626 |
| gwascentral | rs10490626 |
| openSNP | rs10490626 |
| 23andMe | rs10490626 |
| SNPshot | rs10490626 |
| SNPdbe | rs10490626 |
| MSV3d | rs10490626 |
| GWAS Ctlg | rs10490626 |
| GMAF | 0.03444 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20858904] Fine Mapping of the INSIG2 Gene Identifies a Variant Associated with Low-Density Lipoprotein Cholesterol and Total ApoB Levels
[PMID 19360016
] INSIG2 SNPs associated with obesity and glucose homeostasis traits in Hispanics: the IRAS Family Study.
| GWAS snp | |
|---|---|
| PMID | [PMID 24097068]
|
| Trait | Cholesterol, total |
| Title | Discovery and refinement of loci associated with lipid levels. |
| Risk Allele | A |
| P-val | 6E-9 |
| Odds Ratio | .04 [NR] unit increase |
