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: rs10759932
rs10759932
TLR4
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.010 1.000 1 2018 2018
dbSNP: rs10759932
rs10759932
TLR4
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18
CUI: C0940937
Disease: precancerous lesions
precancerous lesions 		0.010 1.000 1 2014 2014
dbSNP: rs10759932
rs10759932
TLR4
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18
CUI: C0085166
Disease: Bacterial Vaginosis
Bacterial Vaginosis 		0.010 1.000 1 2008 2008
dbSNP: rs10759932
rs10759932
TLR4
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.010 < 0.001 1 2016 2016
dbSNP: rs200829864
rs200829864
TLR4
9 117704494 missense variant G/A;T snv 2.1E-05
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		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: C0003615
Disease: Appendicitis
Appendicitis 		0.010 1.000 1 2004 2004
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: rs1191926239
rs1191926239
TLR4
0.807 0.200 9 117704539 missense variant C/G snv 4.0E-06
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.010 1.000 1 2015 2015
dbSNP: rs1191926239
rs1191926239
TLR4
0.807 0.200 9 117704539 missense variant C/G snv 4.0E-06
CUI: C0017086
Disease: Gangrene
Gangrene 		0.010 1.000 1 2004 2004
dbSNP: rs1191926239
rs1191926239
TLR4
0.807 0.200 9 117704539 missense variant C/G snv 4.0E-06
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.010 1.000 1 2015 2015
dbSNP: rs1191926239
rs1191926239
TLR4
0.807 0.200 9 117704539 missense variant C/G snv 4.0E-06
CUI: C0856169
Disease: Endothelial dysfunction
Endothelial dysfunction 		0.010 1.000 1 2013 2013
dbSNP: rs1191926239
rs1191926239
TLR4
0.807 0.200 9 117704539 missense variant C/G snv 4.0E-06
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy 		0.010 1.000 1 2009 2009
dbSNP: rs1347844721
rs1347844721
TLR4
1.000 0.080 9 117704565 missense variant G/A;C snv 4.0E-06
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		0.010 1.000 1 2015 2015
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: 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
dbSNP: rs1927911
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.010 1.000 1 2009 2009
dbSNP: rs1927911
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2014 2014
dbSNP: rs1927911
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62
CUI: C4048328
Disease: cervical cancer
cervical cancer 		0.010 1.000 1 2019 2019
dbSNP: rs1927911
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.010 1.000 1 2008 2008
dbSNP: rs1927911
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 1.000 1 2013 2013
dbSNP: rs1927911
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62
CUI: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis 		0.010 < 0.001 1 2019 2019
dbSNP: rs1927911
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 1.000 1 2014 2014
dbSNP: rs1927911
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62
CUI: C0027947
Disease: Neutropenia
Neutropenia 		0.010 1.000 1 2011 2011