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