rs2479415
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2479415(A;A) |
Make rs2479415(A;G) |
Make rs2479415(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 55033072 |
is a | snp |
is | mentioned by |
dbSNP | rs2479415 |
dbSNP (classic) | rs2479415 |
ClinGen | rs2479415 |
ebi | rs2479415 |
HLI | rs2479415 |
Exac | rs2479415 |
Gnomad | rs2479415 |
Varsome | rs2479415 |
LitVar | rs2479415 |
Map | rs2479415 |
PheGenI | rs2479415 |
Biobank | rs2479415 |
1000 genomes | rs2479415 |
hgdp | rs2479415 |
ensembl | rs2479415 |
geneview | rs2479415 |
scholar | rs2479415 |
rs2479415 | |
pharmgkb | rs2479415 |
gwascentral | rs2479415 |
openSNP | rs2479415 |
23andMe | rs2479415 |
SNPshot | rs2479415 |
SNPdbe | rs2479415 |
MSV3d | rs2479415 |
GWAS Ctlg | rs2479415 |
GMAF | 0.4063 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 22460556] Common and Low-Frequency Genetic Variants in the PCSK9 Locus Influence Circulating PCSK9 Levels