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: rs4986790
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C3536715
Disease: AA amyloidosis
AA amyloidosis 		0.010 1.000 1 2011 2011
dbSNP: rs4986791
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02
CUI: C3536715
Disease: AA amyloidosis
AA amyloidosis 		0.010 1.000 1 2011 2011
dbSNP: rs4986791
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02
CUI: C1112209
Disease: Abdominal Infection
Abdominal Infection 		0.010 1.000 1 2013 2013
dbSNP: rs4986790
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0151332
Disease: Active tuberculosis
Active tuberculosis 		0.020 1.000 2 2007 2010
dbSNP: rs4986790
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0001311
Disease: Acute bronchiolitis
Acute bronchiolitis 		0.010 < 0.001 1 2015 2015
dbSNP: rs4986791
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02
CUI: C0001311
Disease: Acute bronchiolitis
Acute bronchiolitis 		0.010 < 0.001 1 2015 2015
dbSNP: rs4986790
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome 		0.010 1.000 1 2003 2003
dbSNP: rs4986791
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02
CUI: C0856825
Disease: Acute GVH disease
Acute GVH disease 		0.010 1.000 1 2006 2006
dbSNP: rs7045953
rs7045953
TLR4
0.925 0.200 9 117723517 3 prime UTR variant A/G snv 0.19
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria 		0.010 1.000 1 2009 2009
dbSNP: rs7045953
rs7045953
TLR4
0.925 0.200 9 117723517 3 prime UTR variant A/G snv 0.19
CUI: C1279945
Disease: Acute interstitial pneumonia
Acute interstitial pneumonia 		0.010 1.000 1 2009 2009
dbSNP: rs4986790
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0085669
Disease: Acute leukemia
Acute leukemia 		0.010 1.000 1 2013 2013
dbSNP: rs4986791
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02
CUI: C0085669
Disease: Acute leukemia
Acute leukemia 		0.010 1.000 1 2013 2013
dbSNP: rs4986790
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C3890941
Disease: Acute Motor Axonal Neuropathy
Acute Motor Axonal Neuropathy 		0.010 1.000 1 2010 2010
dbSNP: rs4986791
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02
CUI: C3890941
Disease: Acute Motor Axonal Neuropathy
Acute Motor Axonal Neuropathy 		0.010 1.000 1 2010 2010
dbSNP: rs1191926239
rs1191926239
TLR4
0.807 0.200 9 117704539 missense variant C/G snv 4.0E-06
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction 		0.010 1.000 1 2013 2013
dbSNP: rs4986790
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0155626
Disease: Acute myocardial infarction
Acute myocardial infarction 		0.010 1.000 1 2007 2007
dbSNP: rs4986790
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis 		0.030 0.667 3 2007 2014
dbSNP: rs4986791
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02
CUI: C0001339
Disease: Acute pancreatitis
Acute pancreatitis 		0.010 < 0.001 1 2014 2014
dbSNP: rs4986791
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02
CUI: C0001342
Disease: Acute periodontitis
Acute periodontitis 		0.030 1.000 3 2008 2015
dbSNP: rs4986790
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0001342
Disease: Acute periodontitis
Acute periodontitis 		0.020 1.000 2 2008 2015
dbSNP: rs4986790
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0520575
Disease: Acute pyelonephritis
Acute pyelonephritis 		0.010 1.000 1 2018 2018
dbSNP: rs16906079
rs16906079
TLR4
9 117712651 missense variant A/G snv 6.5E-04 4.3E-04
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma 		0.010 1.000 1 2006 2006
dbSNP: rs4986790
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma 		0.010 1.000 1 2011 2011
dbSNP: rs1927911
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62
CUI: C0001430
Disease: Adenoma
Adenoma 		0.010 1.000 1 2018 2018
dbSNP: rs7873784
rs7873784
TLR4
0.752 0.440 9 117716658 3 prime UTR variant G/A;C;T snv
CUI: C0001430
Disease: Adenoma
Adenoma 		0.010 1.000 1 2018 2018