rs679899
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs679899(A;A) |
| Make rs679899(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 21028042 |
| Gene | APOB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs679899 |
| dbSNP (classic) | rs679899 |
| ClinGen | rs679899 |
| ebi | rs679899 |
| HLI | rs679899 |
| Exac | rs679899 |
| Gnomad | rs679899 |
| Varsome | rs679899 |
| LitVar | rs679899 |
| Map | rs679899 |
| PheGenI | rs679899 |
| Biobank | rs679899 |
| 1000 genomes | rs679899 |
| hgdp | rs679899 |
| ensembl | rs679899 |
| geneview | rs679899 |
| scholar | rs679899 |
| rs679899 | |
| pharmgkb | rs679899 |
| gwascentral | rs679899 |
| openSNP | rs679899 |
| 23andMe | rs679899 |
| SNPshot | rs679899 |
| SNPdbe | rs679899 |
| MSV3d | rs679899 |
| GWAS Ctlg | rs679899 |
| GMAF | 0.4917 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19282863] Association of candidate gene polymorphisms with chronic kidney disease in Japanese individuals with hypertension
[PMID 20018037
] Mendelian randomization in family data.
| ClinVar | |
|---|---|
| Risk | rs679899(A;A) |
| Alt | rs679899(A;A) |
| Reference | Rs679899(G;G) |
| Significance | Other |
| Disease | not specified Familial hypercholesterolemia Familial hypobetalipoproteinemia |
| Variation | info |
| Gene | APOB |
| CLNDBN | not specified Familial hypercholesterolemia Familial hypobetalipoproteinemia |
| Reversed | 0 |
| HGVS | NC_000002.11:g.21250914G>A |
| CLNSRC | Instituto Nacional de Saúde Doutor Ricardo Jorge |
| CLNACC | RCV000116384.4, RCV000256290.2, RCV000295735.1, |
