LIPG, lipase G, endothelial type, 9388

N. diseases: 62; N. variants: 18
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: rs770572030
rs770572030 		0.827 0.160 18 49581427 missense variant T/A;C snv 4.0E-06; 4.0E-06
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.060 0.833 6 2008 2019
dbSNP: rs770572030
rs770572030 		0.827 0.160 18 49581427 missense variant T/A;C snv 4.0E-06; 4.0E-06
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.030 1.000 3 2014 2019
dbSNP: rs770572030
rs770572030 		0.827 0.160 18 49581427 missense variant T/A;C snv 4.0E-06; 4.0E-06
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.030 1.000 3 2014 2019
dbSNP: rs77960347
rs77960347 		18 49583585 missense variant A/C;G snv 4.0E-06; 8.7E-03
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 3 2014 2018
dbSNP: rs12970066
rs12970066 		18 49580782 intron variant C/A;G snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 2 2016 2018
dbSNP: rs77960347
rs77960347 		18 49583585 missense variant A/C;G snv 4.0E-06; 8.7E-03
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 2 2018 2018
dbSNP: rs3813082
rs3813082 		1.000 0.040 18 49561673 5 prime UTR variant A/C;G snv 1.9E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs4245232
rs4245232 		18 49560628 upstream gene variant A/C;T snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs4245232
rs4245232 		18 49560628 upstream gene variant A/C;T snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs770572030
rs770572030 		0.827 0.160 18 49581427 missense variant T/A;C snv 4.0E-06; 4.0E-06
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy 		Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs770572030
rs770572030 		0.827 0.160 18 49581427 missense variant T/A;C snv 4.0E-06; 4.0E-06
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2007 2007
dbSNP: rs77960347
rs77960347 		18 49583585 missense variant A/C;G snv 4.0E-06; 8.7E-03
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs77960347
rs77960347 		18 49583585 missense variant A/C;G snv 4.0E-06; 8.7E-03
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms 		Behavior and Behavior Mechanisms 0.010 1.000 1 2017 2017
dbSNP: rs77960347
rs77960347 		18 49583585 missense variant A/C;G snv 4.0E-06; 8.7E-03
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs77960347
rs77960347 		18 49583585 missense variant A/C;G snv 4.0E-06; 8.7E-03
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs874565
rs874565 		18 49562320 synonymous variant C/A;T snv 9.4E-03
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs874565
rs874565 		18 49562320 synonymous variant C/A;T snv 9.4E-03
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs874565
rs874565 		18 49562320 synonymous variant C/A;T snv 9.4E-03
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs201922257
rs201922257 		18 49569492 missense variant C/T snv 1.7E-04 2.7E-04
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2017 2017
dbSNP: rs201922257
rs201922257 		18 49569492 missense variant C/T snv 1.7E-04 2.7E-04
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2017 2017
dbSNP: rs149615216
rs149615216 		18 49579658 intron variant C/T snv 5.6E-03
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 2 2017 2018
dbSNP: rs149615216
rs149615216 		18 49579658 intron variant C/T snv 5.6E-03
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 2 2015 2018
dbSNP: rs9958734
rs9958734 		18 49592028 3 prime UTR variant T/C snv 8.4E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2017 2017
dbSNP: rs12966382
rs12966382 		18 49559070 upstream gene variant C/T snv 0.11
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs12966382
rs12966382 		18 49559070 upstream gene variant C/T snv 0.11
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012