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: rs2149356
rs2149356
TLR4
0.742 0.360 9 117711921 intron variant T/G snv 0.54
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
Glaucoma, Primary Open Angle 		0.040 1.000 4 2012 2020
dbSNP: rs1927911
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.030 1.000 3 2013 2015
dbSNP: rs1927911
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy 		0.020 1.000 2 2014 2015
dbSNP: rs1927911
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder) 		0.020 1.000 2 2013 2014
dbSNP: rs2149356
rs2149356
TLR4
0.742 0.360 9 117711921 intron variant T/G snv 0.54
CUI: C0152136
Disease: Low Tension Glaucoma
Low Tension Glaucoma 		0.020 1.000 2 2008 2019
dbSNP: rs2149356
rs2149356
TLR4
0.742 0.360 9 117711921 intron variant T/G snv 0.54
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		0.020 1.000 2 2015 2019
dbSNP: rs11536878
rs11536878
TLR4
0.827 0.240 9 117709275 intron variant C/A snv 9.5E-02
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 < 0.001 1 2014 2014
dbSNP: rs11536878
rs11536878
TLR4
0.827 0.240 9 117709275 intron variant C/A snv 9.5E-02
CUI: C0017154
Disease: Gastritis, Atrophic
Gastritis, Atrophic 		0.010 < 0.001 1 2014 2014
dbSNP: rs11536878
rs11536878
TLR4
0.827 0.240 9 117709275 intron variant C/A snv 9.5E-02
CUI: C0850666
Disease: Infection caused by Helicobacter pylori
Infection caused by Helicobacter pylori 		0.010 1.000 1 2014 2014
dbSNP: rs11536878
rs11536878
TLR4
0.827 0.240 9 117709275 intron variant C/A snv 9.5E-02
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.010 < 0.001 1 2014 2014
dbSNP: rs11536878
rs11536878
TLR4
0.827 0.240 9 117709275 intron variant C/A snv 9.5E-02
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.010 < 0.001 1 2015 2015
dbSNP: rs11536879
rs11536879
TLR4
1.000 0.040 9 117709933 intron variant A/C;G;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2019 2019
dbSNP: rs12377632
rs12377632
TLR4
0.827 0.120 9 117710452 intron variant T/A;C snv
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.010 1.000 1 2014 2014
dbSNP: rs12377632
rs12377632
TLR4
0.827 0.120 9 117710452 intron variant T/A;C snv
CUI: C0017601
Disease: Glaucoma
Glaucoma 		0.010 1.000 1 2017 2017
dbSNP: rs12377632
rs12377632
TLR4
0.827 0.120 9 117710452 intron variant T/A;C snv
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
Glaucoma, Primary Open Angle 		0.010 1.000 1 2017 2017
dbSNP: rs12377632
rs12377632
TLR4
0.827 0.120 9 117710452 intron variant T/A;C snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.010 1.000 1 2014 2014
dbSNP: rs12377632
rs12377632
TLR4
0.827 0.120 9 117710452 intron variant T/A;C snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.010 1.000 1 2011 2011
dbSNP: rs1927907
rs1927907
TLR4
0.790 0.320 9 117710486 intron variant C/T snv 0.18
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		0.010 1.000 1 2019 2019
dbSNP: rs1927907
rs1927907
TLR4
0.790 0.320 9 117710486 intron variant C/T snv 0.18
CUI: C0004096
Disease: Asthma
Asthma 		0.010 1.000 1 2011 2011
dbSNP: rs1927907
rs1927907
TLR4
0.790 0.320 9 117710486 intron variant C/T snv 0.18
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
Henoch-Schoenlein Purpura 		0.010 1.000 1 2017 2017
dbSNP: rs1927907
rs1927907
TLR4
0.790 0.320 9 117710486 intron variant C/T snv 0.18
CUI: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis 		0.010 1.000 1 2016 2016
dbSNP: rs1927907
rs1927907
TLR4
0.790 0.320 9 117710486 intron variant C/T snv 0.18
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
Benign Prostatic Hyperplasia 		0.010 1.000 1 2019 2019
dbSNP: rs1927907
rs1927907
TLR4
0.790 0.320 9 117710486 intron variant C/T snv 0.18
CUI: C1145670
Disease: Respiratory Failure
Respiratory Failure 		0.010 1.000 1 2017 2017
dbSNP: rs1927907
rs1927907
TLR4
0.790 0.320 9 117710486 intron variant C/T snv 0.18
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		0.010 1.000 1 2016 2016
dbSNP: rs1927911
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62
CUI: C1456868
Disease: Diabetic foot ulcer
Diabetic foot ulcer 		0.010 1.000 1 2013 2013