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rs4539842

From SNPedia

Orientationplus
Stabilizedplus
Make rs4539842(A;A)
Make rs4539842(A;T)
Make rs4539842(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position48755625
GeneLHCGR, STON1-GTF2A1L
is asnp
is mentioned by
dbSNPrs4539842
ebirs4539842
HLIrs4539842
Exacrs4539842
Varsomers4539842
Maprs4539842
PheGenIrs4539842
hapmaprs4539842
1000 genomesrs4539842
hgdprs4539842
ensemblrs4539842
gopubmedrs4539842
geneviewrs4539842
scholarrs4539842
googlers4539842
pharmgkbrs4539842
gwascentralrs4539842
openSNPrs4539842
23andMers4539842
23andMe allrs4539842
SNP Nexus

SNPshotrs4539842
SNPdbers4539842
MSV3drs4539842
GWAS Ctlgrs4539842
Max Magnitude

[PMID 23883350OA-icon.png] Association between the luteinizing hormone/chorionic gonadotropin receptor (LHCGR) rs4073366 polymorphism and ovarian hyperstimulation syndrome during controlled ovarian hyperstimulation [PMID 18300940] Polymorphisms of the luteinizing hormone/chorionic gonadotropin receptor gene: association with maldescended testes and male infertility.


[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.