rs2268361

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
google	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