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: rs2294426
rs2294426 		1.000 0.080 6 11729849 intron variant A/G;T snv
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases 0.800 1.000 1 2011 2011
dbSNP: rs6903956
rs6903956 		0.763 0.160 6 11774350 intron variant A/G snv 0.65
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.720 1.000 3 2011 2015
dbSNP: rs210894
rs210894 		6 11731766 non coding transcript exon variant T/A snv 0.43
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs2235418
rs2235418 		6 11732590 intron variant C/T snv 0.31
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2012 2012
dbSNP: rs760788
rs760788 		6 11770472 intron variant C/G;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs9469930
rs9469930 		6 11720988 intron variant G/A snv 0.68
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs6903956
rs6903956 		0.763 0.160 6 11774350 intron variant A/G snv 0.65
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.050 1.000 5 2011 2015
dbSNP: rs6903956
rs6903956 		0.763 0.160 6 11774350 intron variant A/G snv 0.65
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.030 1.000 3 2012 2015
dbSNP: rs1018383
rs1018383 		1.000 0.040 6 11784092 intron variant C/T snv 0.76
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs11966356
rs11966356 		1.000 0.040 6 11783014 intron variant C/T snv 0.74
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs6903956
rs6903956 		0.763 0.160 6 11774350 intron variant A/G snv 0.65
CUI: C0348944
Disease: Hyperuricemia without signs of inflammatory arthritis and tophaceous disease
Hyperuricemia without signs of inflammatory arthritis and tophaceous disease 		Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs6903956
rs6903956 		0.763 0.160 6 11774350 intron variant A/G snv 0.65
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs6903956
rs6903956 		0.763 0.160 6 11774350 intron variant A/G snv 0.65
CUI: C0281782
Disease: asymptomatic hyperuricemia
asymptomatic hyperuricemia 		0.010 1.000 1 2015 2015
dbSNP: rs6903956
rs6903956 		0.763 0.160 6 11774350 intron variant A/G snv 0.65
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs6903956
rs6903956 		0.763 0.160 6 11774350 intron variant A/G snv 0.65
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs6903956
rs6903956 		0.763 0.160 6 11774350 intron variant A/G snv 0.65
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs6903956
rs6903956 		0.763 0.160 6 11774350 intron variant A/G snv 0.65
CUI: C0740394
Disease: Hyperuricemia
Hyperuricemia 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2015 2015
dbSNP: rs7753407
rs7753407 		1.000 0.040 6 11780108 intron variant G/A snv 0.75
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2015 2015