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: rs6922269
rs6922269 		0.807 0.200 6 150931849 intron variant G/A snv 0.35
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.020 0.500 2 2009 2014
dbSNP: rs751421713
rs751421713 		6 151013801 missense variant A/G snv 8.0E-06
CUI: C0027794
Disease: Neural Tube Defects
Neural Tube Defects 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases 0.020 1.000 2 2006 2009
dbSNP: rs11754661
rs11754661 		0.851 0.120 6 150885942 intron variant G/A;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.820 0.667 3 2010 2011
dbSNP: rs6922269
rs6922269 		0.807 0.200 6 150931849 intron variant G/A snv 0.35
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.040 1.000 4 2010 2015
dbSNP: rs6922269
rs6922269 		0.807 0.200 6 150931849 intron variant G/A snv 0.35
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.830 1.000 5 2007 2014