Source: ALL

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: rs9340799
rs9340799
0.583 0.680 6 151842246 intron variant A/G snv 0.32
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.020 1.000 2 2005 2013
dbSNP: rs9340799
rs9340799
0.583 0.680 6 151842246 intron variant A/G snv 0.32
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.010 1.000 1 2005 2005
dbSNP: rs9340799
rs9340799
0.583 0.680 6 151842246 intron variant A/G snv 0.32
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.070 0.857 7 2007 2020
dbSNP: rs9340799
rs9340799
0.583 0.680 6 151842246 intron variant A/G snv 0.32
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.070 0.857 7 2007 2020
dbSNP: rs9340799
rs9340799
0.583 0.680 6 151842246 intron variant A/G snv 0.32
Ventricular Fibrillation, Paroxysmal Familial, 1
0.010 1.000 1 2007 2007
dbSNP: rs9340799
rs9340799
0.583 0.680 6 151842246 intron variant A/G snv 0.32
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
0.020 1.000 2 2008 2009
dbSNP: rs9340799
rs9340799
0.583 0.680 6 151842246 intron variant A/G snv 0.32
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium
0.020 1.000 2 2008 2009
dbSNP: rs9340799
rs9340799
0.583 0.680 6 151842246 intron variant A/G snv 0.32
CUI: C0151744
Disease: Myocardial Ischemia
Myocardial Ischemia
0.010 < 0.001 1 2008 2008
dbSNP: rs9340799
rs9340799
0.583 0.680 6 151842246 intron variant A/G snv 0.32
CUI: C0263746
Disease: Osteoarthritis of the hand
Osteoarthritis of the hand
0.020 0.500 2 2009 2014
dbSNP: rs9340799
rs9340799
0.583 0.680 6 151842246 intron variant A/G snv 0.32
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
0.010 1.000 1 2009 2009
dbSNP: rs9340799
rs9340799
0.583 0.680 6 151842246 intron variant A/G snv 0.32
CUI: C0028754
Disease: Obesity
Obesity
0.010 1.000 1 2009 2009
dbSNP: rs9340799
rs9340799
0.583 0.680 6 151842246 intron variant A/G snv 0.32
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.010 1.000 1 2009 2009
dbSNP: rs9340799
rs9340799
0.583 0.680 6 151842246 intron variant A/G snv 0.32
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.020 0.500 2 2010 2015
dbSNP: rs9340799
rs9340799
0.583 0.680 6 151842246 intron variant A/G snv 0.32
CUI: C0011570
Disease: Mental Depression
Mental Depression
0.030 1.000 3 2011 2017
dbSNP: rs9340799
rs9340799
0.583 0.680 6 151842246 intron variant A/G snv 0.32
CUI: C0344315
Disease: Depressed mood
Depressed mood
0.030 1.000 3 2011 2017
dbSNP: rs9340799
rs9340799
0.583 0.680 6 151842246 intron variant A/G snv 0.32
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.030 1.000 3 2011 2017
dbSNP: rs9340799
rs9340799
0.583 0.680 6 151842246 intron variant A/G snv 0.32
CUI: C0039585
Disease: Androgen-Insensitivity Syndrome
Androgen-Insensitivity Syndrome
0.010 1.000 1 2011 2011
dbSNP: rs9340799
rs9340799
0.583 0.680 6 151842246 intron variant A/G snv 0.32
CUI: C0006145
Disease: Breast Diseases
Breast Diseases
0.010 1.000 1 2011 2011
dbSNP: rs9340799
rs9340799
0.583 0.680 6 151842246 intron variant A/G snv 0.32
CUI: C1328504
Disease: Hormone refractory prostate cancer
Hormone refractory prostate cancer
0.010 1.000 1 2011 2011
dbSNP: rs9340799
rs9340799
0.583 0.680 6 151842246 intron variant A/G snv 0.32
CUI: C0349231
Disease: Phobic anxiety disorder
Phobic anxiety disorder
0.010 1.000 1 2011 2011
dbSNP: rs9340799
rs9340799
0.583 0.680 6 151842246 intron variant A/G snv 0.32
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.050 0.800 5 2012 2017
dbSNP: rs9340799
rs9340799
0.583 0.680 6 151842246 intron variant A/G snv 0.32
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.050 0.800 5 2012 2017
dbSNP: rs9340799
rs9340799
0.583 0.680 6 151842246 intron variant A/G snv 0.32
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.020 1.000 2 2012 2012
dbSNP: rs9340799
rs9340799
0.583 0.680 6 151842246 intron variant A/G snv 0.32
CUI: C0003467
Disease: Anxiety
Anxiety
0.010 1.000 1 2012 2012
dbSNP: rs9340799
rs9340799
0.583 0.680 6 151842246 intron variant A/G snv 0.32
CUI: C0235782
Disease: Gallbladder Carcinoma
Gallbladder Carcinoma
0.010 1.000 1 2012 2012