rs1119582
From SNPedia
Merged into | rs465384 |
Orientation | minus |
Stabilized | minus |
Make rs1119582(A;A) |
Make rs1119582(A;G) |
Make rs1119582(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 125907327 |
is a | snp |
is | mentioned by |
dbSNP | rs1119582 |
dbSNP (classic) | rs1119582 |
ClinGen | rs1119582 |
ebi | rs1119582 |
HLI | rs1119582 |
Exac | rs1119582 |
Gnomad | rs1119582 |
Varsome | rs1119582 |
LitVar | rs1119582 |
Map | rs1119582 |
PheGenI | rs1119582 |
Biobank | rs1119582 |
1000 genomes | rs1119582 |
hgdp | rs1119582 |
ensembl | rs1119582 |
geneview | rs1119582 |
scholar | rs1119582 |
rs1119582 | |
pharmgkb | rs1119582 |
gwascentral | rs1119582 |
openSNP | rs1119582 |
23andMe | rs1119582 |
SNPshot | rs1119582 |
SNPdbe | rs1119582 |
MSV3d | rs1119582 |
GWAS Ctlg | rs1119582 |
Status | Merged into rs465384 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 17903293] |
Trait | Select biomarker traits |
Title | Genome-wide association with select biomarker traits in the Framingham Heart Study |
Risk Allele | |
P-val | 9.9999999999999995E-7 |
Odds Ratio | NR NR |