rs2268361
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2268361(A;A) |
Make rs2268361(A;G) |
Make rs2268361(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 48974473 |
Gene | FSHR |
is a | snp |
is | mentioned by |
dbSNP | rs2268361 |
dbSNP (classic) | rs2268361 |
ClinGen | rs2268361 |
ebi | rs2268361 |
HLI | rs2268361 |
Exac | rs2268361 |
Gnomad | rs2268361 |
Varsome | rs2268361 |
LitVar | rs2268361 |
Map | rs2268361 |
PheGenI | rs2268361 |
Biobank | rs2268361 |
1000 genomes | rs2268361 |
hgdp | rs2268361 |
ensembl | rs2268361 |
geneview | rs2268361 |
scholar | rs2268361 |
rs2268361 | |
pharmgkb | rs2268361 |
gwascentral | rs2268361 |
openSNP | rs2268361 |
23andMe | rs2268361 |
SNPshot | rs2268361 |
SNPdbe | rs2268361 |
MSV3d | rs2268361 |
GWAS Ctlg | rs2268361 |
GMAF | 0.4959 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22885925] |
Trait | Polycystic ovary syndrome |
Title | Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome. |
Risk Allele | C |
P-val | 1E-12 |
Odds Ratio | 1.15 [NR] |
[PMID 16864747] Mutation of the follicle-stimulating hormone receptor gene 5'-untranslated region associated with female hypertension.
[PMID 25904635] Han Chinese polycystic ovary syndrome risk variants in women of European ancestry: relationship to FSH levels and glucose tolerance