Variant: rs11031006 

    present in Gene: LOC105376607
    present in Chromosome: 11
    Position on Chromosome: 30204981
    Alleles of this Variant: G/A

rs11031006 in LOC105376607 gene and Age at menarche PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.

rs11031006 in LOC105376607 gene and Age at menopause PMID 26414677 2015 Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair.

rs11031006 in LOC105376607 gene and Luteinizing hormone measurement PMID 26284813 2015 The same chr 11p14.1 SNP, rs11031006, in the region of the follicle-stimulating hormone B polypeptide (FSHB) gene strongly associates with PCOS diagnosis and luteinizing hormone levels.

rs11031006 in LOC105376607 gene and Menorrhagia PMID 31649266 2019 Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis.

rs11031006 in LOC105376607 gene and Plexiform leiomyoma PMID 31649266 2019 Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis.

rs11031006 in LOC105376607 gene and Polycystic Ovary Syndrome PMID 26416764 2015 Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome.

PMID 26284813 2015 The same chr 11p14.1 SNP, rs11031006, in the region of the follicle-stimulating hormone B polypeptide (FSHB) gene strongly associates with PCOS diagnosis and luteinizing hormone levels.

rs11031006 in LOC105376607 gene and Uterine Fibroids PMID 31649266 2019 Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis.