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: rs1805087
rs1805087 		0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia 		0.040 1.000 4 2002 2012
dbSNP: rs1039659576
rs1039659576 		0.689 0.520 1 236803473 missense variant A/G snv
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia 		0.020 1.000 2 2009 2012
dbSNP: rs1805087
rs1805087 		0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.020 1.000 2 1999 2004
dbSNP: rs201765376
rs201765376 		0.732 0.360 1 236838504 synonymous variant C/T snv 1.6E-05 1.4E-05
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia 		0.020 1.000 2 2002 2012
dbSNP: rs1039659576
rs1039659576 		0.689 0.520 1 236803473 missense variant A/G snv
CUI: C1853238
Disease: Conotruncal defect
Conotruncal defect 		0.010 1.000 1 2018 2018
dbSNP: rs1805087
rs1805087 		0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C3146250
Disease: Stage III Colorectal Cancer AJCC v7
Stage III Colorectal Cancer AJCC v7 		0.010 1.000 1 2011 2011
dbSNP: rs1805087
rs1805087 		0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C2712907
Disease: obsolete Combined hyperlipidemia
obsolete Combined hyperlipidemia 		0.010 1.000 1 2008 2008
dbSNP: rs1805087
rs1805087 		0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C1963943
Disease: Atherothrombosis
Atherothrombosis 		0.010 1.000 1 2002 2002
dbSNP: rs1805087
rs1805087 		0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C0424101
Disease: Inattention
Inattention 		0.010 1.000 1 2017 2017
dbSNP: rs2275565
rs2275565 		1 236885376 intron variant G/T snv 0.29
CUI: C2242817
Disease: Homocysteine measurement
Homocysteine measurement 		0.800 1.000 1 2013 2013
dbSNP: rs4659744
rs4659744 		0.925 0.080 1 236896158 intron variant G/C snv 0.34
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 1.000 1 2010 2010
dbSNP: rs757891309
rs757891309 		0.882 0.120 1 236850389 missense variant C/A;T snv 4.0E-06; 4.0E-06
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia 		0.010 1.000 1 2012 2012
dbSNP: rs121913578
rs121913578 		0.851 0.280 1 236895470 missense variant C/T snv 6.4E-05 8.4E-05
CUI: C1848580
Disease: Decreased methionine synthase activity
Decreased methionine synthase activity 		0.700 0
dbSNP: rs1805087
rs1805087 		0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C0344315
Disease: Depressed mood
Depressed mood 		Behavior and Behavior Mechanisms 0.010 1.000 1 2008 2008
dbSNP: rs1805087
rs1805087 		0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior 		Behavior and Behavior Mechanisms 0.010 1.000 1 2018 2018
dbSNP: rs1805087
rs1805087 		0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C0011570
Disease: Mental Depression
Mental Depression 		Behavior and Behavior Mechanisms 0.010 1.000 1 2008 2008
dbSNP: rs757522886
rs757522886 		1 236885125 missense variant C/T snv 8.0E-06
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms 		Behavior and Behavior Mechanisms 0.010 1.000 1 2016 2016
dbSNP: rs757891309
rs757891309 		0.882 0.120 1 236850389 missense variant C/A;T snv 4.0E-06; 4.0E-06
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms 		Behavior and Behavior Mechanisms 0.010 1.000 1 2011 2011
dbSNP: rs1805087
rs1805087 		0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.080 1.000 8 1999 2017
dbSNP: rs1805087
rs1805087 		0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.080 1.000 8 2001 2019
dbSNP: rs1805087
rs1805087 		0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.030 1.000 3 2001 2005
dbSNP: rs1039659576
rs1039659576 		0.689 0.520 1 236803473 missense variant A/G snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.020 1.000 2 2010 2013
dbSNP: rs142648132
rs142648132 		0.827 0.160 1 236816521 missense variant G/A;C;T snv 8.4E-04; 2.4E-05
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.020 1.000 2 2010 2012
dbSNP: rs1805087
rs1805087 		0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21
CUI: C0042373
Disease: Vascular Diseases
Vascular Diseases 		Cardiovascular Diseases 0.020 0.500 2 1997 1999
dbSNP: rs1050993
rs1050993 		1.000 0.040 1 236899005 3 prime UTR variant A/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 1.000 1 2019 2019