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rs2091787

From SNPedia

Orientationminus
Stabilizedminus
Make rs2091787(C;C)
Make rs2091787(C;T)
Make rs2091787(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position49017420
GeneFSHR
is asnp
is mentioned by
dbSNPrs2091787
ebirs2091787
HLIrs2091787
Exacrs2091787
Varsomers2091787
Maprs2091787
PheGenIrs2091787
hapmaprs2091787
1000 genomesrs2091787
hgdprs2091787
ensemblrs2091787
gopubmedrs2091787
geneviewrs2091787
scholarrs2091787
googlers2091787
pharmgkbrs2091787
gwascentralrs2091787
openSNPrs2091787
23andMers2091787
23andMe allrs2091787
SNP Nexus

SNPshotrs2091787
SNPdbers2091787
MSV3drs2091787
GWAS Ctlgrs2091787
GMAF0.3848
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 23884663OA-icon.png] Alterations of the FSH and LH receptor genes and evaluation of sperm ultrastructure in men with idiopathic hypergonadotropic hypogonadism