rs7300312 in LOC105370003 gene and Adenocarcinoma of large intestine

PMID 30510241 2019 Discovery of common and rare genetic risk variants for colorectal cancer.

PMID 31089142 2019 Association analyses identify 31 new risk loci for colorectal cancer susceptibility.

rs7300312 in LOC105370003 gene and Adenoma of large intestine

PMID 30510241 2019 Discovery of common and rare genetic risk variants for colorectal cancer.

rs2161877 in LOC105370003 gene and Adolescent idiopathic scoliosis

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs2460488 in LOC105370003 gene and Body Height

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

rs6490030 in LOC105370003 gene and Body mass index

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

rs1292011 in LOC105370003 gene and Breast Carcinoma

PMID 25751625 2015 Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer.

PMID 29059683 2017 Association analysis identifies 65 new breast cancer risk loci.

PMID 23535729 2013 Large-scale genotyping identifies 41 new loci associated with breast cancer risk.

rs7300312 in LOC105370003 gene and COLORECTAL CANCER, SUSCEPTIBILITY TO, 1

PMID 30510241 2019 Discovery of common and rare genetic risk variants for colorectal cancer.

PMID 31089142 2019 Association analyses identify 31 new risk loci for colorectal cancer susceptibility.

rs7300312 in LOC105370003 gene and COLORECTAL CANCER, SUSCEPTIBILITY TO, 10

PMID 30510241 2019 Discovery of common and rare genetic risk variants for colorectal cancer.

PMID 31089142 2019 Association analyses identify 31 new risk loci for colorectal cancer susceptibility.

rs7300312 in LOC105370003 gene and COLORECTAL CANCER, SUSCEPTIBILITY TO, 12

PMID 30510241 2019 Discovery of common and rare genetic risk variants for colorectal cancer.

PMID 31089142 2019 Association analyses identify 31 new risk loci for colorectal cancer susceptibility.

rs7300312 in LOC105370003 gene and COLORECTAL CANCER, SUSCEPTIBILITY TO, 3

PMID 30510241 2019 Discovery of common and rare genetic risk variants for colorectal cancer.

PMID 31089142 2019 Association analyses identify 31 new risk loci for colorectal cancer susceptibility.

rs7958945 in LOC105370003 gene and Chronic Obstructive Airway Disease

PMID 30804561 2019 Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations.

rs7300312 in LOC105370003 gene and Colorectal Carcinoma

PMID 30510241 2019 Discovery of common and rare genetic risk variants for colorectal cancer.

PMID 31089142 2019 Association analyses identify 31 new risk loci for colorectal cancer susceptibility.

rs7300312 in LOC105370003 gene and Colorectal Neoplasms

PMID 30510241 2019 Discovery of common and rare genetic risk variants for colorectal cancer.

PMID 31089142 2019 Association analyses identify 31 new risk loci for colorectal cancer susceptibility.

rs10850519 in LOC105370003 gene and Diastolic blood pressure

PMID 28135244 2017 Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk.

PMID 29455858 2018 A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure.

PMID 27841878 2017 Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation.

PMID 25249183 2015 Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension.

rs1463833 in LOC105370003 gene and Height

PMID 20400458 2010 Genome-wide association of anthropometric traits in African- and African-derived populations.

rs11067763 in LOC105370003 gene and Hypertensive disease

PMID 25249183 2015 Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension.

rs11610288 in LOC105370003 gene and Leukemia, Myelocytic, Acute

PMID 27903959 2017 Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.

rs1292011 in LOC105370003 gene and Malignant neoplasm of breast

PMID 23535729 2013 Large-scale genotyping identifies 41 new loci associated with breast cancer risk.

rs7300312 in LOC105370003 gene and Malignant neoplasm of large intestine

PMID 30510241 2019 Discovery of common and rare genetic risk variants for colorectal cancer.

PMID 31089142 2019 Association analyses identify 31 new risk loci for colorectal cancer susceptibility.

rs7300312 in LOC105370003 gene and Malignant tumor of colon

PMID 30510241 2019 Discovery of common and rare genetic risk variants for colorectal cancer.

PMID 31089142 2019 Association analyses identify 31 new risk loci for colorectal cancer susceptibility.

rs2161877 in LOC105370003 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3

PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11067762 in LOC105370003 gene and Systolic Pressure

PMID 29455858 2018 A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure.

PMID 25249183 2015 Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension.

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