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rs1922464

From SNPedia

Orientationminus
Stabilizedminus
Make rs1922464(C;C)
Make rs1922464(C;G)
Make rs1922464(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position48997291
GeneFSHR
is asnp
is mentioned by
dbSNPrs1922464
ebirs1922464
HLIrs1922464
Exacrs1922464
Varsomers1922464
Maprs1922464
PheGenIrs1922464
hapmaprs1922464
1000 genomesrs1922464
hgdprs1922464
ensemblrs1922464
gopubmedrs1922464
geneviewrs1922464
scholarrs1922464
googlers1922464
pharmgkbrs1922464
gwascentralrs1922464
openSNPrs1922464
23andMers1922464
23andMe allrs1922464
SNP Nexus

SNPshotrs1922464
SNPdbers1922464
MSV3drs1922464
GWAS Ctlgrs1922464
GMAF0.4596
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 23884663OA-icon.png] Alterations of the FSH and LH receptor genes and evaluation of sperm ultrastructure in men with idiopathic hypergonadotropic hypogonadism