rs4629571
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4629571(A;A) |
Make rs4629571(A;G) |
Make rs4629571(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 75362479 |
Gene | HMGCR |
is a | snp |
is | mentioned by |
dbSNP | rs4629571 |
dbSNP (classic) | rs4629571 |
ClinGen | rs4629571 |
ebi | rs4629571 |
HLI | rs4629571 |
Exac | rs4629571 |
Gnomad | rs4629571 |
Varsome | rs4629571 |
LitVar | rs4629571 |
Map | rs4629571 |
PheGenI | rs4629571 |
Biobank | rs4629571 |
1000 genomes | rs4629571 |
hgdp | rs4629571 |
ensembl | rs4629571 |
geneview | rs4629571 |
scholar | rs4629571 |
rs4629571 | |
pharmgkb | rs4629571 |
gwascentral | rs4629571 |
openSNP | rs4629571 |
23andMe | rs4629571 |
SNPshot | rs4629571 |
SNPdbe | rs4629571 |
MSV3d | rs4629571 |
GWAS Ctlg | rs4629571 |
GMAF | 0.09826 |
Max Magnitude | 0 |
[PMID 19327767] Variants in the HMG-CoA reductase (HMGCR) gene influence component phenotypes in polycystic ovary syndrome
[PMID 33167740] Association of NCP1L1 and HMGCR Gene Polymorphisms with Major Adverse Cardiac and Cerebrovascular Events in Patients with Three-Vessel Disease.