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