rs783147
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs783147(C;C) |
| Make rs783147(C;T) |
| Make rs783147(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 160716958 |
| Gene | PLG |
| is a | snp |
| is | mentioned by |
| dbSNP | rs783147 |
| dbSNP (classic) | rs783147 |
| ClinGen | rs783147 |
| ebi | rs783147 |
| HLI | rs783147 |
| Exac | rs783147 |
| Gnomad | rs783147 |
| Varsome | rs783147 |
| LitVar | rs783147 |
| Map | rs783147 |
| PheGenI | rs783147 |
| Biobank | rs783147 |
| 1000 genomes | rs783147 |
| hgdp | rs783147 |
| ensembl | rs783147 |
| geneview | rs783147 |
| scholar | rs783147 |
| rs783147 | |
| pharmgkb | rs783147 |
| gwascentral | rs783147 |
| openSNP | rs783147 |
| 23andMe | rs783147 |
| SNPshot | rs783147 |
| SNPdbe | rs783147 |
| MSV3d | rs783147 |
| GWAS Ctlg | rs783147 |
| GMAF | 0.4114 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21900290 |
| Trait | |
| Title | Genetic variants, plasma lipoprotein(a) levels, and risk of cardiovascular morbidity and mortality among two prospective cohorts of type 2 diabetes. |
| Risk Allele | A |
| P-val | 3E-17 |
| Odds Ratio | 0.3000 [0.22-0.38] mg/dL decrease |
[PMID 21078622
] Conventional and Mendelian randomization analyses suggest no association between lipoprotein(a) and early atherosclerosis: the Young Finns Study.
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 6
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
