rs3775290, TLR3

N. diseases: 15
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.742 0.280 4 186083063 missense variant C/A;T snv 0.30 0.020 1.000 2 2011 2016
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.742 0.280 4 186083063 missense variant C/A;T snv 0.30 0.020 1.000 2 2011 2016
Complete atrioventricular block
CUI: C0151517
Disease: Complete atrioventricular block
96 0.742 0.280 4 186083063 missense variant C/A;T snv 0.30 0.020 1.000 2 2015 2016
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.742 0.280 4 186083063 missense variant C/A;T snv 0.30 0.020 1.000 2 2016 2019
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.742 0.280 4 186083063 missense variant C/A;T snv 0.30 0.020 1.000 2 2015 2019
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.742 0.280 4 186083063 missense variant C/A;T snv 0.30 0.020 1.000 2 2011 2016
Cytomegalovirus Infections
CUI: C0010823
Disease: Cytomegalovirus Infections
26 0.742 0.280 4 186083063 missense variant C/A;T snv 0.30 0.010 1.000 1 2017 2017
Hepatitis B, Chronic
CUI: C0524909
Disease: Hepatitis B, Chronic
84 0.742 0.280 4 186083063 missense variant C/A;T snv 0.30 0.010 1.000 1 2016 2016
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.742 0.280 4 186083063 missense variant C/A;T snv 0.30 0.010 1.000 1 2019 2019
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.742 0.280 4 186083063 missense variant C/A;T snv 0.30 0.010 1.000 1 2015 2015
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.742 0.280 4 186083063 missense variant C/A;T snv 0.30 0.010 1.000 1 2014 2014
Meningitis, Bacterial
CUI: C0085437
Disease: Meningitis, Bacterial
16 0.742 0.280 4 186083063 missense variant C/A;T snv 0.30 0.010 1.000 1 2017 2017
Osteoarthritis, Knee
CUI: C0409959
Disease: Osteoarthritis, Knee
150 0.742 0.280 4 186083063 missense variant C/A;T snv 0.30 0.010 1.000 1 2013 2013
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.742 0.280 4 186083063 missense variant C/A;T snv 0.30 0.010 1.000 1 2014 2014
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.742 0.280 4 186083063 missense variant C/A;T snv 0.30 0.010 1.000 1 2016 2016