Gene: LOC105376607

Alternate names for this Gene:

Gene Summary:

Gene is located in Chromosome:

Location in Chromosome :

Description of this Gene:

Type of Gene:

rs11031005 in LOC105376607 gene and Age at menarche PMID 27182965 2016 Detection and interpretation of shared genetic influences on 42 human traits.

PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.

rs11031005 in LOC105376607 gene and Age at menopause PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.

PMID 26414677 2015 Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair.

rs74485684 in LOC105376607 gene and Endometriosis PMID 28537267 2017 Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism.

rs11031005 in LOC105376607 gene and Follicle stimulating hormone measurement PMID 26014426 2016 Genome-wide association study with 1000 genomes imputation identifies signals for nine sex hormone-related phenotypes.

rs11031002 in LOC105376607 gene and Hormone measurement PMID 26014426 2016 Genome-wide association study with 1000 genomes imputation identifies signals for nine sex hormone-related phenotypes.

rs11031002 in LOC105376607 gene and Luteinizing hormone measurement PMID 26014426 2016 Genome-wide association study with 1000 genomes imputation identifies signals for nine sex hormone-related phenotypes.

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.

rs11031005 in LOC105376607 gene and Polycystic Ovary Syndrome PMID 30566500 2018 Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria.

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.

rs35229181 in LOC105376607 gene and Uric acid measurement (procedure) PMID 31578528 2019 Target genes, variants, tissues and transcriptional pathways influencing human serum urate 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.