rs9370867
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9370867(A;A) |
Make rs9370867(A;G) |
Make rs9370867(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 16145094 |
Gene | MYLIP |
is a | snp |
is | mentioned by |
dbSNP | rs9370867 |
dbSNP (classic) | rs9370867 |
ClinGen | rs9370867 |
ebi | rs9370867 |
HLI | rs9370867 |
Exac | rs9370867 |
Gnomad | rs9370867 |
Varsome | rs9370867 |
LitVar | rs9370867 |
Map | rs9370867 |
PheGenI | rs9370867 |
Biobank | rs9370867 |
1000 genomes | rs9370867 |
hgdp | rs9370867 |
ensembl | rs9370867 |
geneview | rs9370867 |
scholar | rs9370867 |
rs9370867 | |
pharmgkb | rs9370867 |
gwascentral | rs9370867 |
openSNP | rs9370867 |
23andMe | rs9370867 |
SNPshot | rs9370867 |
SNPdbe | rs9370867 |
MSV3d | rs9370867 |
GWAS Ctlg | rs9370867 |
GMAF | 0.258 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 21765216] The N342S MYLIP polymorphism is associated with high total cholesterol and increased LDL receptor degradation in humans
[PMID 25927920] IDOL N342S Variant, Atherosclerosis Progression and Cardiovascular Disorders in the Italian General Population
[PMID 32868861] IDOL gene variant is associated with hyperlipidemia in Han population in Xinjiang, China.