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: rs749495848
rs749495848
TLR4
9 117713210 missense variant A/C;G snv 4.0E-06
CUI: C0025303
Disease: Meningococcal Infections
Meningococcal Infections 		0.010 1.000 1 2013 2013
dbSNP: rs749495848
rs749495848
TLR4
9 117713210 missense variant A/C;G snv 4.0E-06
CUI: C0021290
Disease: Neonatal disorder
Neonatal disorder 		0.010 1.000 1 2006 2006
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: 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: 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: 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
dbSNP: rs1927911
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		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: C0007785
Disease: Cerebral Infarction
Cerebral Infarction 		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: C0031099
Disease: Periodontitis
Periodontitis 		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: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		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: C0242172
Disease: Pelvic Inflammatory Disease
Pelvic Inflammatory Disease 		0.010 1.000 1 2012 2012
dbSNP: rs1927911
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.010 < 0.001 1 2017 2017
dbSNP: rs1927911
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		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: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		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: C0001430
Disease: Adenoma
Adenoma 		0.010 1.000 1 2018 2018