rs150468
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs150468(A;C) |
| Make rs150468(C;C) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 16 |
| Position | 16158143 |
| Gene | ABCC6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs150468 |
| dbSNP (classic) | rs150468 |
| ClinGen | rs150468 |
| ebi | rs150468 |
| HLI | rs150468 |
| Exac | rs150468 |
| Gnomad | rs150468 |
| Varsome | rs150468 |
| LitVar | rs150468 |
| Map | rs150468 |
| PheGenI | rs150468 |
| Biobank | rs150468 |
| 1000 genomes | rs150468 |
| hgdp | rs150468 |
| ensembl | rs150468 |
| geneview | rs150468 |
| scholar | rs150468 |
| rs150468 | |
| pharmgkb | rs150468 |
| gwascentral | rs150468 |
| openSNP | rs150468 |
| 23andMe | rs150468 |
| SNPshot | rs150468 |
| SNPdbe | rs150468 |
| MSV3d | rs150468 |
| GWAS Ctlg | rs150468 |
| GMAF | 0.1033 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 20855565
] Common genetic variation in multiple metabolic pathways influences susceptibility to low HDL-cholesterol and coronary heart disease
| ClinVar | |
|---|---|
| Risk | rs150468(C;C) |
| Alt | rs150468(C;C) |
| Reference | Rs150468(A;A) |
| Significance | Untested |
| Disease | |
| Variation | info |
| Gene | ABCC6 |
| CLNDBN | |
| Reversed | 1 |
| HGVS | NC_000016.9:g.16252000T>G |
| CLNSRC | |
| CLNACC | |
