rs4149338
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs4149338(C;T) |
| Make rs4149338(T;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 9 |
| Position | 104783622 |
| Gene | ABCA1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4149338 |
| dbSNP (classic) | rs4149338 |
| ClinGen | rs4149338 |
| ebi | rs4149338 |
| HLI | rs4149338 |
| Exac | rs4149338 |
| Gnomad | rs4149338 |
| Varsome | rs4149338 |
| LitVar | rs4149338 |
| Map | rs4149338 |
| PheGenI | rs4149338 |
| Biobank | rs4149338 |
| 1000 genomes | rs4149338 |
| hgdp | rs4149338 |
| ensembl | rs4149338 |
| geneview | rs4149338 |
| scholar | rs4149338 |
| rs4149338 | |
| pharmgkb | rs4149338 |
| gwascentral | rs4149338 |
| openSNP | rs4149338 |
| 23andMe | rs4149338 |
| SNPshot | rs4149338 |
| SNPdbe | rs4149338 |
| MSV3d | rs4149338 |
| GWAS Ctlg | rs4149338 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 26722555
] Association of ATP-binding cassette transporter A1 gene polymorphisms with plasma lipid variability and coronary heart disease risk.
| ClinVar | |
|---|---|
| Risk | rs4149338(T;T) |
| Alt | rs4149338(T;T) |
| Reference | Rs4149338(C;C) |
| Significance | Non-pathogenic |
| Disease | Familial High Density Lipoprotein Deficiency Tangier disease |
| Variation | info |
| Gene | ABCA1 |
| CLNDBN | Familial High Density Lipoprotein Deficiency Tangier disease |
| Reversed | 1 |
| HGVS | NC_000009.11:g.107545903G>A |
| CLNSRC | |
| CLNACC | RCV000286965.1, RCV000379060.1, |
