rs1044317
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1044317(A;A) |
Make rs1044317(A;G) |
Make rs1044317(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 21 |
Position | 42296791 |
Gene | ABCG1 |
is a | snp |
is | mentioned by |
dbSNP | rs1044317 |
dbSNP (classic) | rs1044317 |
ClinGen | rs1044317 |
ebi | rs1044317 |
HLI | rs1044317 |
Exac | rs1044317 |
Gnomad | rs1044317 |
Varsome | rs1044317 |
LitVar | rs1044317 |
Map | rs1044317 |
PheGenI | rs1044317 |
Biobank | rs1044317 |
1000 genomes | rs1044317 |
hgdp | rs1044317 |
ensembl | rs1044317 |
geneview | rs1044317 |
scholar | rs1044317 |
rs1044317 | |
pharmgkb | rs1044317 |
gwascentral | rs1044317 |
openSNP | rs1044317 |
23andMe | rs1044317 |
SNPshot | rs1044317 |
SNPdbe | rs1044317 |
MSV3d | rs1044317 |
GWAS Ctlg | rs1044317 |
GMAF | 0.41 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 21722899] A polymorphism in the ABCG1 promoter is functionally associated with coronary artery disease in a Chinese Han population
[PMID 17187964] ABCG1 gene variants in suicidal behavior and aggression-related traits.