rs1028771
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs1028771(A;C) |
Make rs1028771(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 183201813 |
Gene | LAMC2 |
is a | snp |
is | mentioned by |
dbSNP | rs1028771 |
dbSNP (classic) | rs1028771 |
ClinGen | rs1028771 |
ebi | rs1028771 |
HLI | rs1028771 |
Exac | rs1028771 |
Gnomad | rs1028771 |
Varsome | rs1028771 |
LitVar | rs1028771 |
Map | rs1028771 |
PheGenI | rs1028771 |
Biobank | rs1028771 |
1000 genomes | rs1028771 |
hgdp | rs1028771 |
ensembl | rs1028771 |
geneview | rs1028771 |
scholar | rs1028771 |
rs1028771 | |
pharmgkb | rs1028771 |
gwascentral | rs1028771 |
openSNP | rs1028771 |
23andMe | rs1028771 |
SNPshot | rs1028771 |
SNPdbe | rs1028771 |
MSV3d | rs1028771 |
GWAS Ctlg | rs1028771 |
GMAF | 0.009183 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21347282] |
Trait | |
Title | Genome-Wide Association Study of Coronary Heart Disease and Its Risk Factors in 8,090 African Americans: The NHLBI CARe Project |
Risk Allele | A |
P-val | 0.000004 |
Odds Ratio | 0.2188 [0.13-0.31] SD decrease |