rs2091787
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2091787(C;C) |
| Make rs2091787(C;T) |
| Make rs2091787(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 49017420 |
| Gene | FSHR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2091787 |
| dbSNP (classic) | rs2091787 |
| ClinGen | rs2091787 |
| ebi | rs2091787 |
| HLI | rs2091787 |
| Exac | rs2091787 |
| Gnomad | rs2091787 |
| Varsome | rs2091787 |
| LitVar | rs2091787 |
| Map | rs2091787 |
| PheGenI | rs2091787 |
| Biobank | rs2091787 |
| 1000 genomes | rs2091787 |
| hgdp | rs2091787 |
| ensembl | rs2091787 |
| geneview | rs2091787 |
| scholar | rs2091787 |
| rs2091787 | |
| pharmgkb | rs2091787 |
| gwascentral | rs2091787 |
| openSNP | rs2091787 |
| 23andMe | rs2091787 |
| SNPshot | rs2091787 |
| SNPdbe | rs2091787 |
| MSV3d | rs2091787 |
| GWAS Ctlg | rs2091787 |
| GMAF | 0.3848 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 23884663
] Alterations of the FSH and LH receptor genes and evaluation of sperm ultrastructure in men with idiopathic hypergonadotropic hypogonadism
