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 |
