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: rs17810546
rs17810546 		0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		Digestive System Diseases; Nutritional and Metabolic Diseases 0.820 1.000 4 2008 2020
dbSNP: rs17810546
rs17810546 		0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02
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 0.810 1.000 3 2013 2015
dbSNP: rs485499
rs485499 		0.925 0.080 3 160028076 intron variant T/C snv 0.29
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.800 1.000 3 2011 2015
dbSNP: rs582537
rs582537 		1.000 0.080 3 159992311 intron variant A/C;G snv
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.800 1.000 2 2012 2017
dbSNP: rs6441286
rs6441286 		0.925 0.080 3 160011091 intron variant T/G snv 0.36
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.800 1.000 2 2009 2010
dbSNP: rs1353248
rs1353248 		0.925 0.120 3 159905770 intron variant C/T snv 0.32
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		Digestive System Diseases; Nutritional and Metabolic Diseases 0.800 1.000 1 2011 2011
dbSNP: rs2366643
rs2366643 		1.000 0.080 3 160018698 intron variant T/C;G snv
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.800 1.000 1 2012 2012
dbSNP: rs2561288
rs2561288 		1.000 0.080 3 159957140 intron variant T/C snv 0.54
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		Digestive System Diseases; Nutritional and Metabolic Diseases 0.800 1.000 1 2011 2011
dbSNP: rs6799788
rs6799788 		1.000 0.040 3 159926508 intron variant A/G snv 0.18
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.800 1.000 1 2013 2013
dbSNP: rs545143
rs545143 		1.000 0.080 3 160014208 intron variant C/A;T snv 0.41
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.700 1.000 2 2012 2012
dbSNP: rs564799
rs564799 		0.925 0.160 3 160011200 intron variant C/T snv 0.33
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.700 1.000 2 2015 2016
dbSNP: rs6441286
rs6441286 		0.925 0.080 3 160011091 intron variant T/G snv 0.36
CUI: C0023892
Disease: Biliary cirrhosis
Biliary cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.700 1.000 2 2009 2010
dbSNP: rs1014486
rs1014486 		1.000 0.080 3 159973324 intron variant T/C snv 0.39
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs11918142
rs11918142 		1.000 0.040 3 160189298 intron variant T/C snv 0.20
CUI: C4021107
Disease: Non-obstructive azoospermia
Non-obstructive azoospermia 		Male Urogenital Diseases 0.700 1.000 1 2011 2011
dbSNP: rs1353248
rs1353248 		0.925 0.120 3 159905770 intron variant C/T snv 0.32
CUI: C0149745
Disease: Oral Ulcer
Oral Ulcer 		Stomatognathic Diseases 0.700 1.000 1 2019 2019
dbSNP: rs1651081
rs1651081 		1.000 0.080 3 160014715 intron variant A/T snv 0.41
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs17810546
rs17810546 		0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs17810546
rs17810546 		0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases 		Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs17810546
rs17810546 		0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs17810546
rs17810546 		0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs1874886
rs1874886 		0.925 0.280 3 160011868 non coding transcript exon variant G/A snv 0.41
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs1874886
rs1874886 		0.925 0.280 3 160011868 non coding transcript exon variant G/A snv 0.41
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 0.700 1.000 1 2016 2016
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