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: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0023418
Disease: leukemia
leukemia
0.020 1.000 2 2012 2013
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0392156
Disease: Akathisia
Akathisia
0.020 1.000 2 2010 2017
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C1868683
Disease: B-CELL MALIGNANCY, LOW-GRADE
B-CELL MALIGNANCY, LOW-GRADE
0.020 1.000 2 2007 2015
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0149925
Disease: Small cell carcinoma of lung
Small cell carcinoma of lung
0.020 1.000 2 2006 2012
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0018798
Disease: Congenital Heart Defects
Congenital Heart Defects
0.020 1.000 2 2011 2013
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C3495949
Disease: Locally advanced breast cancer
Locally advanced breast cancer
0.020 1.000 2 2003 2008
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.020 1.000 2 2014 2016
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0220615
Disease: Adult Acute Myeloblastic Leukemia
Adult Acute Myeloblastic Leukemia
0.020 0.500 2 2006 2008
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.020 < 0.001 2 2005 2020
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome
0.020 1.000 2 2009 2015
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
Human immunodeficiency virus (HIV) II infection category B1
0.020 1.000 2 2006 2011
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0030805
Disease: Bullous pemphigoid
Bullous pemphigoid
0.020 0.500 2 2017 2018
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders
0.020 0.500 2 2003 2010
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome
0.020 1.000 2 2014 2014
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.020 1.000 2 2014 2015
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0344315
Disease: Depressed mood
Depressed mood
0.020 1.000 2 2014 2015
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0011570
Disease: Mental Depression
Mental Depression
0.020 1.000 2 2014 2015
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.020 1.000 2 2016 2017
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0027726
Disease: Nephrotic Syndrome
Nephrotic Syndrome
0.020 1.000 2 2011 2013
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.020 1.000 2 2011 2014
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C3266262
Disease: Multiple Chronic Conditions
Multiple Chronic Conditions
0.020 1.000 2 2007 2012
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.020 1.000 2 2013 2014
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
Infection caused by Helicobacter pylori
0.020 1.000 2 2007 2008
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
CUI: C0018816
Disease: Heart Septal Defects
Heart Septal Defects
0.020 1.000 2 2013 2014
dbSNP: rs1045642
rs1045642
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50
Diabetes Mellitus, Non-Insulin-Dependent
0.020 1.000 2 2012 2017