LIPC, lipase C, hepatic type, 3990

N. diseases: 120; N. variants: 95
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: rs12912415
rs12912415 		15 58429248 intron variant A/G snv 0.11
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs12914035
rs12914035 		15 58438690 intron variant A/G snv 0.10
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs17269348
rs17269348 		0.925 0.040 15 58532442 intron variant A/G snv 7.8E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs17269348
rs17269348 		0.925 0.040 15 58532442 intron variant A/G snv 7.8E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs261332
rs261332 		0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332 		0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0337438
Disease: Glucose measurement
Glucose measurement 		0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332 		0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332 		0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332 		0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332 		0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0011847
Disease: Diabetes
Diabetes 		Endocrine System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332 		0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs261332
rs261332 		0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332 		0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs261332
rs261332 		0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332 		0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332 		0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level 		0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332 		0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332 		0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332 		0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.700 1.000 1 2008 2008
dbSNP: rs261332
rs261332 		0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0018801
Disease: Heart failure
Heart failure 		Cardiovascular Diseases 0.700 1.000 1 2016 2016
dbSNP: rs261332
rs261332 		0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2016 2016
dbSNP: rs261338
rs261338 		15 58442806 intron variant A/G snv 0.83
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs261338
rs261338 		15 58442806 intron variant A/G snv 0.83
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs261338
rs261338 		15 58442806 intron variant A/G snv 0.83
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs261338
rs261338 		15 58442806 intron variant A/G snv 0.83
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012