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: rs10127775
rs10127775 		1 230160042 intron variant A/G;T snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs10864728
rs10864728 		1 230169168 intron variant A/G snv 0.50
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs17315646
rs17315646 		1 230159560 intron variant C/A;G snv 0.45
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs7022
rs7022 		1 230281918 3 prime UTR variant C/G;T snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs7549029
rs7549029 		1 230117659 intron variant G/A snv 0.42
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs10127775
rs10127775 		1 230160042 intron variant A/G;T snv
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		Nutritional and Metabolic Diseases; Cardiovascular Diseases 0.700 1.000 1 2012 2012
dbSNP: rs4846914
rs4846914 		0.925 0.080 1 230159944 intron variant G/A snv 0.45
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2010 2010
dbSNP: rs12040273
rs12040273 		0.882 0.040 1 230063651 intron variant C/T snv 0.28
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2144300
rs2144300 		0.882 0.040 1 230159169 intron variant C/T snv 0.44
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs12040273
rs12040273 		0.882 0.040 1 230063651 intron variant C/T snv 0.28
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 < 0.001 1 2018 2018
dbSNP: rs2144300
rs2144300 		0.882 0.040 1 230159169 intron variant C/T snv 0.44
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs2281719
rs2281719 		1.000 0.040 1 230161913 intron variant C/T snv 0.45
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs2144300
rs2144300 		0.882 0.040 1 230159169 intron variant C/T snv 0.44
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.710 1.000 2 2011 2013
dbSNP: rs12040273
rs12040273 		0.882 0.040 1 230063651 intron variant C/T snv 0.28
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs4846914
rs4846914 		0.925 0.080 1 230159944 intron variant G/A snv 0.45
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs16850871
rs16850871 		1 230083723 intron variant A/G snv 0.11
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement 		0.700 1.000 1 2018 2018
dbSNP: rs7513659
rs7513659 		1 230090639 intron variant G/A snv 8.5E-02
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement 		0.700 1.000 1 2018 2018
dbSNP: rs10489615
rs10489615 		1 230169242 intron variant A/C;G snv
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		0.700 1.000 1 2017 2017
dbSNP: rs10864726
rs10864726 		1 230160406 intron variant C/T snv 0.45
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		0.700 1.000 1 2017 2017
dbSNP: rs4846914
rs4846914 		0.925 0.080 1 230159944 intron variant G/A snv 0.45
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 9 2008 2019
dbSNP: rs2144300
rs2144300 		0.882 0.040 1 230159169 intron variant C/T snv 0.44
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 5 2008 2018
dbSNP: rs4846918
rs4846918 		1 230164840 intron variant C/G;T snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 2 2012 2012
dbSNP: rs4846923
rs4846923 		1 230171476 intron variant T/G snv 0.72
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 2 2015 2018
dbSNP: rs10127775
rs10127775 		1 230160042 intron variant A/G;T snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2019 2019
dbSNP: rs10489615
rs10489615 		1 230169242 intron variant A/C;G snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 1 2010 2010