rs4758685
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs4758685(C;C) |
| Make rs4758685(C;T) |
| Make rs4758685(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 122142295 |
| Gene | MLXIP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4758685 |
| dbSNP (classic) | rs4758685 |
| ClinGen | rs4758685 |
| ebi | rs4758685 |
| HLI | rs4758685 |
| Exac | rs4758685 |
| Gnomad | rs4758685 |
| Varsome | rs4758685 |
| LitVar | rs4758685 |
| Map | rs4758685 |
| PheGenI | rs4758685 |
| Biobank | rs4758685 |
| 1000 genomes | rs4758685 |
| hgdp | rs4758685 |
| ensembl | rs4758685 |
| geneview | rs4758685 |
| scholar | rs4758685 |
| rs4758685 | |
| pharmgkb | rs4758685 |
| gwascentral | rs4758685 |
| openSNP | rs4758685 |
| 23andMe | rs4758685 |
| SNPshot | rs4758685 |
| SNPdbe | rs4758685 |
| MSV3d | rs4758685 |
| GWAS Ctlg | rs4758685 |
| GMAF | 0.4936 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 23840567
] The Association Study between Twenty One Polymorphisms in Seven Candidate Genes and Coronary Heart Diseases in Chinese Han Population
