HOXC6, homeobox C6, 3223

N. diseases: 80; N. variants: 14
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11614913
rs11614913 		0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Hemic and Lymphatic Diseases 0.010 < 0.001 1 2015 2015
dbSNP: rs11614913
rs11614913 		0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34
CUI: C0220630
Disease: Adult Liver Carcinoma
Adult Liver Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs12319419
rs12319419 		12 54026992 intron variant G/C snv 0.30
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs4759319
rs4759319 		12 54030947 intron variant G/C;T snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs7308105
rs7308105 		12 54030339 3 prime UTR variant T/C snv 0.38
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs11614913
rs11614913 		0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34
CUI: C0003165
Disease: Anthracosis
Anthracosis 		Respiratory Tract Diseases 0.010 1.000 1 2010 2010
dbSNP: rs11614913
rs11614913 		0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34
CUI: C0003864
Disease: Arthritis
Arthritis 		Musculoskeletal Diseases 0.020 0.500 2 2013 2019
dbSNP: rs11614913
rs11614913 		0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34
CUI: C0403823
Disease: Asthenozoospermia
Asthenozoospermia 		Male Urogenital Diseases 0.010 1.000 1 2016 2016
dbSNP: rs11614913
rs11614913 		0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.020 0.500 2 2011 2016
dbSNP: rs11614913
rs11614913 		0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34
CUI: C0340076
Disease: Asthmatic pulmonary eosinophilia
Asthmatic pulmonary eosinophilia 		Respiratory Tract Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs11614913
rs11614913 		0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs11614913
rs11614913 		0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34
CUI: C0004509
Disease: Azoospermia
Azoospermia 		Male Urogenital Diseases 0.010 1.000 1 2016 2016
dbSNP: rs11614913
rs11614913 		0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs11614913
rs11614913 		0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.040 0.750 4 2011 2017
dbSNP: rs736825
rs736825 		12 54023792 intron variant C/G;T snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2012 2012
dbSNP: rs736825
rs736825 		12 54023792 intron variant C/G;T snv
CUI: C0177804
Disease: Bone Mineral Density Test
Bone Mineral Density Test 		0.700 1.000 1 2012 2012
dbSNP: rs11614913
rs11614913 		0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.100 0.913 23 2009 2018
dbSNP: rs185070757
rs185070757 		0.925 0.080 12 53991774 mature miRNA variant T/G snv 4.0E-06
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2014 2014
dbSNP: rs11614913
rs11614913 		0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34
CUI: C0751075
Disease: Cancer of Digestive System
Cancer of Digestive System 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs11614913
rs11614913 		0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34
CUI: C0751571
Disease: Cancer of Urinary Tract
Cancer of Urinary Tract 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2017 2017
dbSNP: rs11614913
rs11614913 		0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.020 1.000 2 2011 2014
dbSNP: rs11614913
rs11614913 		0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.040 0.750 4 2011 2017
dbSNP: rs11614913
rs11614913 		0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		Neoplasms; Respiratory Tract Diseases 0.100 0.944 18 2009 2018
dbSNP: rs11614913
rs11614913 		0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic 		Cardiovascular Diseases 0.010 1.000 1 2010 2010
dbSNP: rs11614913
rs11614913 		0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.010 1.000 1 2015 2015