Variant: rs10936599 

    present in Gene: MYNN
    present in Chromosome: 3
    Position on Chromosome: 169774313
    Alleles of this Variant: C/T

rs10936599 in MYNN gene and Adenocarcinoma of large intestine PMID 20972440 2010 Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33.

rs10936599 in MYNN gene and COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 PMID 20972440 2010 Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33.

rs10936599 in MYNN gene and COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 PMID 20972440 2010 Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33.

rs10936599 in MYNN gene and COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 PMID 20972440 2010 Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33.

rs10936599 in MYNN gene and COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 PMID 20972440 2010 Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33.

rs10936599 in MYNN gene and Carcinoma of bladder PMID 24163127 2014 Genome-wide association study identifies multiple loci associated with bladder cancer risk.

rs10936599 in MYNN gene and Celiac Disease PMID 20190752 2010 Multiple common variants for celiac disease influencing immune gene expression.

rs10936599 in MYNN gene and Chronic Lymphocytic Leukemia PMID 24292274 2014 A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia.

rs10936599 in MYNN gene and Colorectal Carcinoma PMID 20972440 2010 We identified associations at four new CRC risk loci: 1q41 (rs6691170, odds ratio (OR) = 1.06, P = 9.55 × 10⁻¹⁰ and rs6687758, OR = 1.09, P = 2.27 × 10⁻⁹, 3q26.2 (rs10936599, OR = 0.93, P = 3.39 × 10⁻⁸), 12q13.13 (rs11169552, OR = 0.92, P = 1.89 × 10⁻¹⁰ and rs7136702, OR = 1.06, P = 4.02 × 10⁻⁸) and 20q13.33 (rs4925386, OR = 0.93, P = 1.89 × 10⁻¹⁰).

rs10936599 in MYNN gene and Colorectal Neoplasms PMID 20972440 2010 Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33.

rs10936599 in MYNN gene and Lung Diseases, Interstitial PMID 23583980 2013 Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.

rs10936599 in MYNN gene and Malignant neoplasm of large intestine PMID 20972440 2010 Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33.

rs10936599 in MYNN gene and Malignant neoplasm of urinary bladder PMID 24163127 2014 Genome-wide association study identifies multiple loci associated with bladder cancer risk.

rs10936599 in MYNN gene and Malignant tumor of colon PMID 20972440 2010 Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33.

rs10936599 in MYNN gene and Multiple Myeloma PMID 23955597 2013 Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk.

rs10936599 in MYNN gene and Multiple Sclerosis PMID 21833088 2011 Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.

rs10936599 in MYNN gene and Small Lymphocytic Lymphoma PMID 24292274 2014 A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia.