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: rs1800470
rs1800470
0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.100 0.933 15 2004 2014
dbSNP: rs1800470
rs1800470
0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.100 0.933 15 2004 2014
dbSNP: rs1800470
rs1800470
0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
0.020 1.000 2 2010 2010
dbSNP: rs1800470
rs1800470
0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 1.000 1 2014 2014
dbSNP: rs1800470
rs1800470
0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.010 1.000 1 2010 2010
dbSNP: rs1800470
rs1800470
0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60
CUI: C0031090
Disease: Periodontal Diseases
Periodontal Diseases
0.010 1.000 1 2014 2014
dbSNP: rs1800470
rs1800470
0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60
CUI: C0333186
Disease: Restenosis
Restenosis
0.010 1.000 1 2015 2015
dbSNP: rs1800470
rs1800470
0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60
CUI: C0017563
Disease: Gingival Diseases
Gingival Diseases
0.010 1.000 1 2014 2014
dbSNP: rs1800470
rs1800470
0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis
0.010 1.000 1 2007 2007
dbSNP: rs1800470
rs1800470
0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome
0.010 1.000 1 2012 2012
dbSNP: rs1800470
rs1800470
0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.010 1.000 1 2006 2006
dbSNP: rs1800470
rs1800470
0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.010 1.000 1 2018 2018
dbSNP: rs1800470
rs1800470
0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60
CUI: C0271183
Disease: Severe myopia
Severe myopia
0.010 1.000 1 2009 2009
dbSNP: rs1800470
rs1800470
0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60
CUI: C1565489
Disease: Renal Insufficiency
Renal Insufficiency
0.010 1.000 1 2000 2000
dbSNP: rs1800470
rs1800470
0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60
CUI: C0011269
Disease: Dementia, Vascular
Dementia, Vascular
0.010 1.000 1 2006 2006
dbSNP: rs1800470
rs1800470
0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60
CUI: C0034067
Disease: Pulmonary Emphysema
Pulmonary Emphysema
0.010 1.000 1 2010 2010
dbSNP: rs1800470
rs1800470
0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60
CUI: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis
0.010 1.000 1 2014 2014
dbSNP: rs1800470
rs1800470
0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy
0.010 1.000 1 2014 2014
dbSNP: rs1800470
rs1800470
0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60
Diabetes Mellitus, Non-Insulin-Dependent
0.010 1.000 1 2016 2016
dbSNP: rs1800470
rs1800470
0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60
CUI: C0018133
Disease: Graft-vs-Host Disease
Graft-vs-Host Disease
0.010 1.000 1 2016 2016
dbSNP: rs1800470
rs1800470
0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
0.010 1.000 1 2016 2016
dbSNP: rs1800470
rs1800470
0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60
Secondary malignant neoplasm of lymph node
0.010 1.000 1 2010 2010
dbSNP: rs1800470
rs1800470
0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60
CUI: C0264545
Disease: Thickening of pleura
Thickening of pleura
0.010 1.000 1 2014 2014
dbSNP: rs1800470
rs1800470
0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60
CUI: C0030920
Disease: Peptic Ulcer
Peptic Ulcer
0.010 1.000 1 2007 2007
dbSNP: rs1800470
rs1800470
0.596 0.643 19 41353016 missense variant G/A,C snp 0.55; 2.4E-04 0.60
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.010 1.000 1 2006 2006