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: rs2234693
rs2234693
0.555 0.680 6 151842200 intron variant T/C snv 0.47
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.100 1.000 11 2007 2020
dbSNP: rs2234693
rs2234693
0.555 0.680 6 151842200 intron variant T/C snv 0.47
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.100 1.000 10 2007 2020
dbSNP: rs2234693
rs2234693
0.555 0.680 6 151842200 intron variant T/C snv 0.47
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.050 0.800 5 2012 2017
dbSNP: rs2234693
rs2234693
0.555 0.680 6 151842200 intron variant T/C snv 0.47
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.050 0.800 5 2012 2017
dbSNP: rs2234693
rs2234693
0.555 0.680 6 151842200 intron variant T/C snv 0.47
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.040 1.000 4 2008 2014
dbSNP: rs2234693
rs2234693
0.555 0.680 6 151842200 intron variant T/C snv 0.47
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.030 1.000 3 2011 2017
dbSNP: rs2234693
rs2234693
0.555 0.680 6 151842200 intron variant T/C snv 0.47
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.030 0.667 3 2005 2013
dbSNP: rs2234693
rs2234693
0.555 0.680 6 151842200 intron variant T/C snv 0.47
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
0.020 1.000 2 2008 2009
dbSNP: rs2234693
rs2234693
0.555 0.680 6 151842200 intron variant T/C snv 0.47
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.020 1.000 2 2009 2013
dbSNP: rs2234693
rs2234693
0.555 0.680 6 151842200 intron variant T/C snv 0.47
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium
0.020 1.000 2 2008 2009
dbSNP: rs2234693
rs2234693
0.555 0.680 6 151842200 intron variant T/C snv 0.47
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.020 0.500 2 2009 2013
dbSNP: rs2234693
rs2234693
0.555 0.680 6 151842200 intron variant T/C snv 0.47
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.020 1.000 2 2010 2018
dbSNP: rs2234693
rs2234693
0.555 0.680 6 151842200 intron variant T/C snv 0.47
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
0.020 1.000 2 2010 2017
dbSNP: rs2234693
rs2234693
0.555 0.680 6 151842200 intron variant T/C snv 0.47
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.020 1.000 2 2009 2018
dbSNP: rs2234693
rs2234693
0.555 0.680 6 151842200 intron variant T/C snv 0.47
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.020 0.500 2 2010 2015
dbSNP: rs2234693
rs2234693
0.555 0.680 6 151842200 intron variant T/C snv 0.47
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis
0.020 1.000 2 2010 2015
dbSNP: rs2234693
rs2234693
0.555 0.680 6 151842200 intron variant T/C snv 0.47
CUI: C0085215
Disease: Ovarian Failure, Premature
Ovarian Failure, Premature
0.020 1.000 2 2014 2015
dbSNP: rs2234693
rs2234693
0.555 0.680 6 151842200 intron variant T/C snv 0.47
CUI: C0025322
Disease: Premature Menopause
Premature Menopause
0.020 1.000 2 2014 2015
dbSNP: rs2234693
rs2234693
0.555 0.680 6 151842200 intron variant T/C snv 0.47
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.020 1.000 2 2005 2009
dbSNP: rs2234693
rs2234693
0.555 0.680 6 151842200 intron variant T/C snv 0.47
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.020 1.000 2 2005 2019
dbSNP: rs2234693
rs2234693
0.555 0.680 6 151842200 intron variant T/C snv 0.47
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.020 1.000 2 2010 2018
dbSNP: rs2234693
rs2234693
0.555 0.680 6 151842200 intron variant T/C snv 0.47
CUI: C0023418
Disease: leukemia
leukemia
0.010 1.000 1 2010 2010
dbSNP: rs2234693
rs2234693
0.555 0.680 6 151842200 intron variant T/C snv 0.47
CUI: C0015230
Disease: Exanthema
Exanthema
0.010 < 0.001 1 2017 2017
dbSNP: rs2234693
rs2234693
0.555 0.680 6 151842200 intron variant T/C snv 0.47
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset
0.010 1.000 1 2012 2012
dbSNP: rs2234693
rs2234693
0.555 0.680 6 151842200 intron variant T/C snv 0.47
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.010 1.000 1 2011 2011