Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1042713
rs1042713
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43
CUI: C0004096
Disease: Asthma
Asthma
0.100 0.921 38 1993 2019
dbSNP: rs1042713
rs1042713
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43
CUI: C0028754
Disease: Obesity
Obesity
0.100 0.786 14 2000 2017
dbSNP: rs1042713
rs1042713
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.100 0.833 12 2001 2015
dbSNP: rs1042713
rs1042713
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
0.060 0.833 6 2010 2018
dbSNP: rs1042713
rs1042713
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.050 1.000 5 2002 2017
dbSNP: rs1042713
rs1042713
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43
CUI: C0018801
Disease: Heart failure
Heart failure
0.040 1.000 4 2007 2018
dbSNP: rs1042713
rs1042713
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure
0.040 1.000 4 2007 2018
dbSNP: rs1042713
rs1042713
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43
Diabetes Mellitus, Non-Insulin-Dependent
0.030 1.000 3 2001 2004
dbSNP: rs1042713
rs1042713
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.030 1.000 3 2005 2010
dbSNP: rs1042713
rs1042713
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.030 0.667 3 2005 2013
dbSNP: rs1042713
rs1042713
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
0.020 1.000 2 2013 2016
dbSNP: rs1042713
rs1042713
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.020 1.000 2 2012 2019
dbSNP: rs1042713
rs1042713
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43
CUI: C0038443
Disease: Stress, Psychological
Stress, Psychological
0.020 1.000 2 2001 2006
dbSNP: rs1042713
rs1042713
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.020 1.000 2 2012 2019
dbSNP: rs1042713
rs1042713
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
0.020 1.000 2 2012 2018
dbSNP: rs1042713
rs1042713
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.020 1.000 2 2005 2008
dbSNP: rs1042713
rs1042713
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43
CUI: C0020615
Disease: Hypoglycemia
Hypoglycemia
0.020 1.000 2 2008 2011
dbSNP: rs1042713
rs1042713
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.020 0.500 2 2005 2012
dbSNP: rs1042713
rs1042713
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.010 1.000 1 2002 2002
dbSNP: rs1042713
rs1042713
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43
CUI: C0030193
Disease: Pain
Pain
0.010 1.000 1 2010 2010
dbSNP: rs1042713
rs1042713
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
0.010 1.000 1 2009 2009
dbSNP: rs1042713
rs1042713
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43
ST segment elevation myocardial infarction
0.010 1.000 1 2009 2009
dbSNP: rs1042713
rs1042713
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.010 1.000 1 2011 2011
dbSNP: rs1042713
rs1042713
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.010 1.000 1 2013 2013
dbSNP: rs1042713
rs1042713
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
0.010 1.000 1 2010 2010