IL12A, interleukin 12A, 3592

N. diseases: 261; N. variants: 7
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: rs2243112
rs2243112 		3 159987881 intron variant G/C snv 5.7E-03
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2243112
rs2243112 		3 159987881 intron variant G/C snv 5.7E-03
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2243112
rs2243112 		3 159987881 intron variant G/C snv 5.7E-03
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2243115
rs2243115 		0.776 0.320 3 159988493 intron variant T/G snv 0.10
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs568408
rs568408 		0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 < 0.001 1 2018 2018
dbSNP: rs582054
rs582054 		0.882 0.160 3 159992214 intron variant A/C;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 < 0.001 1 2018 2018
dbSNP: rs568408
rs568408 		0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16
CUI: C0020179
Disease: Huntington Disease
Huntington Disease 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders 0.030 1.000 3 2012 2017
dbSNP: rs568408
rs568408 		0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.020 1.000 2 2011 2013
dbSNP: rs568408
rs568408 		0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.010 1.000 1 2017 2017
dbSNP: rs568408
rs568408 		0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.030 0.667 3 2011 2017
dbSNP: rs2243115
rs2243115 		0.776 0.320 3 159988493 intron variant T/G snv 0.10
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.020 1.000 2 2011 2016
dbSNP: rs2243115
rs2243115 		0.776 0.320 3 159988493 intron variant T/G snv 0.10
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs2243115
rs2243115 		0.776 0.320 3 159988493 intron variant T/G snv 0.10
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs2243115
rs2243115 		0.776 0.320 3 159988493 intron variant T/G snv 0.10
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs2243115
rs2243115 		0.776 0.320 3 159988493 intron variant T/G snv 0.10
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs568408
rs568408 		0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs568408
rs568408 		0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs568408
rs568408 		0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs568408
rs568408 		0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs568408
rs568408 		0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16
CUI: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs2243115
rs2243115 		0.776 0.320 3 159988493 intron variant T/G snv 0.10
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		Infections 0.010 1.000 1 2010 2010
dbSNP: rs2243115
rs2243115 		0.776 0.320 3 159988493 intron variant T/G snv 0.10
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.030 0.667 3 2009 2017
dbSNP: rs2243115
rs2243115 		0.776 0.320 3 159988493 intron variant T/G snv 0.10
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.030 0.667 3 2009 2017
dbSNP: rs568408
rs568408 		0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.030 0.667 3 2009 2017
dbSNP: rs568408
rs568408 		0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.030 0.667 3 2009 2017