rs4073366
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs4073366(C;C) |
| Make rs4073366(C;G) |
| Make rs4073366(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 48755483 |
| Gene | LHCGR, STON1-GTF2A1L |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4073366 |
| dbSNP (classic) | rs4073366 |
| ClinGen | rs4073366 |
| ebi | rs4073366 |
| HLI | rs4073366 |
| Exac | rs4073366 |
| Gnomad | rs4073366 |
| Varsome | rs4073366 |
| LitVar | rs4073366 |
| Map | rs4073366 |
| PheGenI | rs4073366 |
| Biobank | rs4073366 |
| 1000 genomes | rs4073366 |
| hgdp | rs4073366 |
| ensembl | rs4073366 |
| geneview | rs4073366 |
| scholar | rs4073366 |
| rs4073366 | |
| pharmgkb | rs4073366 |
| gwascentral | rs4073366 |
| openSNP | rs4073366 |
| 23andMe | rs4073366 |
| SNPshot | rs4073366 |
| SNPdbe | rs4073366 |
| MSV3d | rs4073366 |
| GWAS Ctlg | rs4073366 |
| GMAF | 0.2048 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 23883350
] Association between the luteinizing hormone/chorionic gonadotropin receptor (LHCGR) rs4073366 polymorphism and ovarian hyperstimulation syndrome during controlled ovarian hyperstimulation
[PMID 18439297] A luteinizing hormone receptor intronic variant is significantly associated with decreased risk of Alzheimer's disease in males carrying an apolipoprotein E epsilon4 allele.
