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rs4073366

From SNPedia

Orientationminus
Stabilizedminus
Make rs4073366(C;C)
Make rs4073366(C;G)
Make rs4073366(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position48755483
GeneLHCGR, STON1-GTF2A1L
is asnp
is mentioned by
dbSNPrs4073366
ebirs4073366
HLIrs4073366
Exacrs4073366
Varsomers4073366
Maprs4073366
PheGenIrs4073366
hapmaprs4073366
1000 genomesrs4073366
hgdprs4073366
ensemblrs4073366
gopubmedrs4073366
geneviewrs4073366
scholarrs4073366
googlers4073366
pharmgkbrs4073366
gwascentralrs4073366
openSNPrs4073366
23andMers4073366
23andMe allrs4073366
SNP Nexus

SNPshotrs4073366
SNPdbers4073366
MSV3drs4073366
GWAS Ctlgrs4073366
GMAF0.2048
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 23883350OA-icon.png] Association between the luteinizing hormone/chorionic gonadotropin receptor (LHCGR) rs4073366 polymorphism and ovarian hyperstimulation syndrome during controlled ovarian hyperstimulation

[PMID 18439297OA-icon.png] A luteinizing hormone receptor intronic variant is significantly associated with decreased risk of Alzheimer's disease in males carrying an apolipoprotein E epsilon4 allele.