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: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.030 1.000 3 2009 2015
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.030 0.667 3 2005 2014
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.030 0.667 3 2005 2014
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.030 1.000 3 2009 2015
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0011269
Disease: Dementia, Vascular
Dementia, Vascular
0.020 1.000 2 2009 2012
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0011570
Disease: Mental Depression
Mental Depression
0.020 1.000 2 2011 2018
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0344315
Disease: Depressed mood
Depressed mood
0.020 1.000 2 2011 2018
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.020 1.000 2 2009 2012
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0014175
Disease: Endometriosis
Endometriosis
0.020 0.500 2 2008 2014
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0018213
Disease: Graves Disease
Graves Disease
0.020 1.000 2 2008 2011
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.020 1.000 2 2011 2018
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0021364
Disease: Male infertility
Male infertility
0.010 1.000 1 2014 2014
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0028754
Disease: Obesity
Obesity
0.010 1.000 1 2009 2009
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.010 1.000 1 2008 2008
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.010 1.000 1 2011 2011
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.010 1.000 1 2014 2014
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0020473
Disease: Hyperlipidemia
Hyperlipidemia
0.010 < 0.001 1 2010 2010
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2012 2012
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.010 1.000 1 2008 2008
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.010 1.000 1 2012 2012
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.010 1.000 1 2017 2017
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.010 1.000 1 2011 2011
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.010 1.000 1 2008 2008
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.010 1.000 1 2012 2012
dbSNP: rs4986938
rs4986938
0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33
CUI: C0023787
Disease: Lipodystrophy
Lipodystrophy
0.010 1.000 1 2012 2012