SCARB1, scavenger receptor class B member 1, 949

N. diseases: 116; N. variants: 34
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: rs10846744
rs10846744 		0.763 0.160 12 124827879 intron variant G/C snv 0.32
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		Cardiovascular Diseases 0.040 0.750 4 2010 2018
dbSNP: rs10846744
rs10846744 		0.763 0.160 12 124827879 intron variant G/C snv 0.32
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		Cardiovascular Diseases 0.040 0.750 4 2010 2018
dbSNP: rs10773112
rs10773112 		12 124853983 intron variant C/T snv 0.63
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 3 2012 2019
dbSNP: rs10846744
rs10846744 		0.763 0.160 12 124827879 intron variant G/C snv 0.32
CUI: C3266262
Disease: Multiple Chronic Conditions
Multiple Chronic Conditions 		Pathological Conditions, Signs and Symptoms 0.030 1.000 3 2010 2018
dbSNP: rs11057830
rs11057830 		0.851 0.040 12 124822507 intron variant G/A snv 0.15
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.710 1.000 3 2017 2019
dbSNP: rs4765623
rs4765623 		0.925 0.120 12 124836304 intron variant C/T snv 0.38
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.810 1.000 3 2011 2017
dbSNP: rs10773105
rs10773105 		12 124799220 intron variant C/T snv 0.63
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 2 2012 2019
dbSNP: rs10846744
rs10846744 		0.763 0.160 12 124827879 intron variant G/C snv 0.32
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.020 1.000 2 2017 2018
dbSNP: rs10846744
rs10846744 		0.763 0.160 12 124827879 intron variant G/C snv 0.32
CUI: C1861453
Disease: Pseudohyperkalemia Cardiff
Pseudohyperkalemia Cardiff 		Nutritional and Metabolic Diseases 0.020 1.000 2 2016 2017
dbSNP: rs10846744
rs10846744 		0.763 0.160 12 124827879 intron variant G/C snv 0.32
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.020 0.500 2 2012 2018
dbSNP: rs10846744
rs10846744 		0.763 0.160 12 124827879 intron variant G/C snv 0.32
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.020 1.000 2 2012 2018
dbSNP: rs11057830
rs11057830 		0.851 0.040 12 124822507 intron variant G/A snv 0.15
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.710 1.000 2 2017 2019
dbSNP: rs10128951
rs10128951 		1.000 0.040 12 124855901 intron variant G/A snv 0.47
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs10744182
rs10744182 		1.000 0.040 12 124833036 intron variant C/T snv 0.49
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 < 0.001 1 2017 2017
dbSNP: rs10773105
rs10773105 		12 124799220 intron variant C/T snv 0.63
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs10773112
rs10773112 		12 124853983 intron variant C/T snv 0.63
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs10846742
rs10846742 		12 124824136 intron variant G/A;T snv
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs10846742
rs10846742 		12 124824136 intron variant G/A;T snv
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.700 1.000 1 2018 2018
dbSNP: rs10846743
rs10846743 		12 124825759 intron variant G/A snv 3.1E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs10846743
rs10846743 		12 124825759 intron variant G/A snv 3.1E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs10846744
rs10846744 		0.763 0.160 12 124827879 intron variant G/C snv 0.32
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs10846744
rs10846744 		0.763 0.160 12 124827879 intron variant G/C snv 0.32
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs10846744
rs10846744 		0.763 0.160 12 124827879 intron variant G/C snv 0.32
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs10846744
rs10846744 		0.763 0.160 12 124827879 intron variant G/C snv 0.32
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs11057830
rs11057830 		0.851 0.040 12 124822507 intron variant G/A snv 0.15
CUI: C1142098
Disease: Vitamin E Assay
Vitamin E Assay 		0.800 1.000 1 2011 2011