rs676210
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs676210(A;A) |
| Make rs676210(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 21008652 |
| Gene | APOB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs676210 |
| dbSNP (classic) | rs676210 |
| ClinGen | rs676210 |
| ebi | rs676210 |
| HLI | rs676210 |
| Exac | rs676210 |
| Gnomad | rs676210 |
| Varsome | rs676210 |
| LitVar | rs676210 |
| Map | rs676210 |
| PheGenI | rs676210 |
| Biobank | rs676210 |
| 1000 genomes | rs676210 |
| hgdp | rs676210 |
| ensembl | rs676210 |
| geneview | rs676210 |
| scholar | rs676210 |
| rs676210 | |
| pharmgkb | rs676210 |
| gwascentral | rs676210 |
| openSNP | rs676210 |
| 23andMe | rs676210 |
| SNPshot | rs676210 |
| SNPdbe | rs676210 |
| MSV3d | rs676210 |
| GWAS Ctlg | rs676210 |
| GMAF | 0.3379 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20724655
] ApoB genetic variants modify the response to fenofibrate: a GOLDN study
[PMID 18296645
] Polymorphisms of genes in the lipid metabolism pathway and risk of biliary tract cancers and stones: a population-based case-control study in Shanghai, China.
[PMID 19474294
] Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.
[PMID 19936222
] Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.
[PMID 23247145] Genome-Wide Association Study Pinpoints a New Functional ApoB Variant Influencing Oxidized LDL Levels but Not Cardiovascular Events: AtheroRemo Consortium
[PMID 22715478] Genotypes associated with lipid metabolism contribute to differences in serum lipid profile of GH-deficient adults before and after GH replacement therapy.
| ClinVar | |
|---|---|
| Risk | rs676210(A;A) rs676210(T;T) |
| Alt | rs676210(A;A) rs676210(T;T) |
| Reference | Rs676210(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.21231524G>A |
| CLNSRC | Instituto Nacional de Saúde Doutor Ricardo Jorge |
| CLNACC | RCV000116390.4, RCV000256326.2, RCV000326889.1, |
