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]