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rs2268361

From SNPedia

Orientationminus
Stabilizedminus
Make rs2268361(A;A)
Make rs2268361(A;G)
Make rs2268361(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position48974473
GeneFSHR
is asnp
is mentioned by
dbSNPrs2268361
ebirs2268361
HLIrs2268361
Exacrs2268361
Varsomers2268361
Maprs2268361
PheGenIrs2268361
hapmaprs2268361
1000 genomesrs2268361
hgdprs2268361
ensemblrs2268361
gopubmedrs2268361
geneviewrs2268361
scholarrs2268361
googlers2268361
pharmgkbrs2268361
gwascentralrs2268361
openSNPrs2268361
23andMers2268361
23andMe allrs2268361
SNP Nexus

SNPshotrs2268361
SNPdbers2268361
MSV3drs2268361
GWAS Ctlgrs2268361
GMAF0.4959
Max Magnitude
? (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