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: 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: rs11536889
rs11536889
TLR4
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.030 1.000 3 2011 2014
dbSNP: rs11536889
rs11536889
TLR4
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.030 1.000 3 2011 2014
dbSNP: rs11536889
rs11536889
TLR4
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.030 1.000 3 2016 2019
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: rs1927914
rs1927914
TLR4
0.732 0.520 9 117702447 upstream gene variant G/A snv 0.52
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.030 1.000 3 2013 2015
dbSNP: rs10759932
rs10759932
TLR4
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		0.020 1.000 2 2019 2019
dbSNP: rs11536889
rs11536889
TLR4
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		0.020 0.500 2 2017 2019
dbSNP: rs11536889
rs11536889
TLR4
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11
CUI: C0036690
Disease: Septicemia
Septicemia 		0.020 1.000 2 2014 2014
dbSNP: rs11536889
rs11536889
TLR4
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.020 1.000 2 2012 2015
dbSNP: rs11536889
rs11536889
TLR4
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		0.020 0.500 2 2017 2019
dbSNP: rs11536889
rs11536889
TLR4
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11
CUI: C4048328
Disease: cervical cancer
cervical cancer 		0.020 0.500 2 2017 2019
dbSNP: rs11536889
rs11536889
TLR4
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.020 1.000 2 2012 2015
dbSNP: rs11536889
rs11536889
TLR4
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.020 0.500 2 2015 2017
dbSNP: rs11536889
rs11536889
TLR4
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.020 0.500 2 2015 2017
dbSNP: rs11536889
rs11536889
TLR4
0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11
CUI: C0243026
Disease: Sepsis
Sepsis 		0.020 1.000 2 2014 2014
dbSNP: rs1554973
rs1554973
TLR4
0.882 0.120 9 117718534 3 prime UTR variant T/C snv 0.38
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.020 1.000 2 2014 2014
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: 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: rs1927914
rs1927914
TLR4
0.732 0.520 9 117702447 upstream gene variant G/A snv 0.52
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy 		0.020 1.000 2 2014 2015
dbSNP: rs1927914
rs1927914
TLR4
0.732 0.520 9 117702447 upstream gene variant G/A snv 0.52
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.020 1.000 2 2015 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: 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: rs7873784
rs7873784
TLR4
0.752 0.440 9 117716658 3 prime UTR variant G/A;C;T snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.020 1.000 2 2013 2020
dbSNP: rs7873784
rs7873784
TLR4
0.752 0.440 9 117716658 3 prime UTR variant G/A;C;T snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.020 1.000 2 2015 2020