IL12A-AS1, IL12A antisense RNA 1, 101928376

N. diseases: 99; N. variants: 54
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: rs568408
rs568408 		0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.030 1.000 3 2009 2017
dbSNP: rs568408
rs568408 		0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.030 1.000 3 2009 2017
dbSNP: rs568408
rs568408 		0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 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: C4048328
Disease: cervical cancer
cervical cancer 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.030 1.000 3 2009 2017
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: 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: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.030 0.667 3 2011 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
dbSNP: rs568408
rs568408 		0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.020 1.000 2 2011 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: C0585442
Disease: Osteosarcoma of bone
Osteosarcoma of bone 		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: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs568408
rs568408 		0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16
CUI: C1332986
Disease: Childhood Osteosarcoma
Childhood Osteosarcoma 		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: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2018 2018
dbSNP: rs568408
rs568408 		0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2018 2018
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: C0206139
Disease: Lichen Planus, Oral
Lichen Planus, Oral 		Skin and Connective Tissue Diseases; Stomatognathic Diseases 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: C1367654
Disease: Marginal Zone B-Cell Lymphoma
Marginal Zone B-Cell Lymphoma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2011 2011
dbSNP: rs568408
rs568408 		0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16
CUI: C0242647
Disease: Mucosa-Associated Lymphoid Tissue Lymphoma
Mucosa-Associated Lymphoid Tissue Lymphoma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2011 2011
dbSNP: rs568408
rs568408 		0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16
CUI: C0029463
Disease: Osteosarcoma
Osteosarcoma 		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: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2011 2011