rs4986791, TLR4

N. diseases: 182
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Polyendocrinopathies, Autoimmune
CUI: C0085409
Disease: Polyendocrinopathies, Autoimmune
21 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.010 1.000 1 2007 2007
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.020 0.500 2 2005 2008
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
110 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.010 1.000 1 2008 2008
Fetal Growth Retardation
CUI: C0015934
Disease: Fetal Growth Retardation
21 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.010 1.000 1 2008 2008
GASTRIC CANCER, INTESTINAL
CUI: C3150911
Disease: GASTRIC CANCER, INTESTINAL
3 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.010 1.000 1 2008 2008
Gastritis, Atrophic
CUI: C0017154
Disease: Gastritis, Atrophic
61 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.010 1.000 1 2008 2008
Gram-negative bacteremia
CUI: C0744471
Disease: Gram-negative bacteremia
2 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.010 1.000 1 2008 2008
HELLP Syndrome
CUI: C0162739
Disease: HELLP Syndrome
10 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.010 1.000 1 2008 2008
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.010 1.000 1 2008 2008
Sarcoidosis
CUI: C0036202
Disease: Sarcoidosis
787 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.010 1.000 1 2009 2009
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.020 1.000 2 2004 2010
Acute Motor Axonal Neuropathy
CUI: C3890941
Disease: Acute Motor Axonal Neuropathy
4 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.010 1.000 1 2010 2010
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.010 1.000 1 2010 2010
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.010 1.000 1 2010 2010
Henoch-Schoenlein Purpura
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
59 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.010 1.000 1 2010 2010
HIV-1 infection
CUI: C2363741
Disease: HIV-1 infection
94 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.010 1.000 1 2010 2010
infertility tubal factor
CUI: C0745287
Disease: infertility tubal factor
4 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.010 1 2010 2010
Neurocysticercosis
CUI: C0338437
Disease: Neurocysticercosis
9 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.010 1.000 1 2010 2010
Reproductive tract infection
CUI: C2314882
Disease: Reproductive tract infection
3 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.010 1 2010 2010
Gallbladder Carcinoma
CUI: C0235782
Disease: Gallbladder Carcinoma
75 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.030 1.000 3 2010 2011
Malignant neoplasm of gallbladder
CUI: C0153452
Disease: Malignant neoplasm of gallbladder
81 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.030 1.000 3 2010 2011
Stage 0 Gallbladder Cancer AJCC v8
CUI: C4525297
Disease: Stage 0 Gallbladder Cancer AJCC v8
56 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.030 1.000 3 2010 2011
Stage IIA Gallbladder Cancer AJCC v8
56 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.030 1.000 3 2010 2011
Stage IIB Gallbladder Cancer AJCC v8
56 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.030 1.000 3 2010 2011
Stage III Gallbladder Cancer AJCC v8
56 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.030 1.000 3 2010 2011