rs150090666
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common/normal |
| (C;T) | 1.5 | Slightly lower odds of developing hypercholesterolemia |
| Make rs150090666(T;T) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 11 |
| Position | 14843853 |
| Gene | PDE3B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs150090666 |
| dbSNP (classic) | rs150090666 |
| ClinGen | rs150090666 |
| ebi | rs150090666 |
| HLI | rs150090666 |
| Exac | rs150090666 |
| Gnomad | rs150090666 |
| Varsome | rs150090666 |
| LitVar | rs150090666 |
| Map | rs150090666 |
| PheGenI | rs150090666 |
| Biobank | rs150090666 |
| 1000 genomes | rs150090666 |
| hgdp | rs150090666 |
| ensembl | rs150090666 |
| geneview | rs150090666 |
| scholar | rs150090666 |
| rs150090666 | |
| pharmgkb | rs150090666 |
| gwascentral | rs150090666 |
| openSNP | rs150090666 |
| 23andMe | rs150090666 |
| SNPshot | rs150090666 |
| SNPdbe | rs150090666 |
| MSV3d | rs150090666 |
| GWAS Ctlg | rs150090666 |
| Max Magnitude | 1.5 |
rs150090666, also known as p.Arg783Ter or R783X, represents a variant in the PDE3B gene on chromosome 11.
Based on a study of UK BioBank participants, carriers of a rs150090666(T) allele are reported to be less likely to be diagnosed with hypercholesterolemia (OR 0.52, p=0.0002) and they are also likely to have a slightly lower body mass index compared to non-carriers.[PMID 29691411
]
