rs6919346
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6919346(C;C) |
| Make rs6919346(C;T) |
| Make rs6919346(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 160539327 |
| Gene | LPA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6919346 |
| dbSNP (classic) | rs6919346 |
| ClinGen | rs6919346 |
| ebi | rs6919346 |
| HLI | rs6919346 |
| Exac | rs6919346 |
| Gnomad | rs6919346 |
| Varsome | rs6919346 |
| LitVar | rs6919346 |
| Map | rs6919346 |
| PheGenI | rs6919346 |
| Biobank | rs6919346 |
| 1000 genomes | rs6919346 |
| hgdp | rs6919346 |
| ensembl | rs6919346 |
| geneview | rs6919346 |
| scholar | rs6919346 |
| rs6919346 | |
| pharmgkb | rs6919346 |
| gwascentral | rs6919346 |
| openSNP | rs6919346 |
| 23andMe | rs6919346 |
| SNPshot | rs6919346 |
| SNPdbe | rs6919346 |
| MSV3d | rs6919346 |
| GWAS Ctlg | rs6919346 |
| GMAF | 0.0854 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19124843 ]
|
| Trait | Plasma Lp (a) levels |
| Title | Genome-wide association study of plasma Lp(a)levels Identifies multiple genes on chromosome 6q |
| Risk Allele | |
| P-val | 4E-11 |
| Odds Ratio | 0.66 [mg/dl decrease] |
[PMID 21127300] Genetic variation in LPAL2, LPA, and PLG predicts plasma lipoprotein(a) level and carotid artery disease risk.
[PMID 21283670] Single-nucleotide polymorphisms in LPA explain most of the ancestry-specific variation in Lp(a) levels in African Americans.
[PMID 21305047] Variation in LPA is associated with Lp(a) levels in three populations from the Third National Health and Nutrition Examination Survey.
