rs187084, TLR9

N. diseases: 35
Source: BEFREE ×
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.
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
213 0.641 0.480 3 52227015 intron variant A/G snv 0.38 0.010 1.000 1 2014 2014
Bacterial Vaginosis
CUI: C0085166
Disease: Bacterial Vaginosis
15 0.641 0.480 3 52227015 intron variant A/G snv 0.38 0.010 1.000 1 2012 2012
Bronchiolitis
CUI: C0006271
Disease: Bronchiolitis
32 0.641 0.480 3 52227015 intron variant A/G snv 0.38 0.010 1.000 1 2016 2016
Cancer of Digestive System
CUI: C0751075
Disease: Cancer of Digestive System
15 0.641 0.480 3 52227015 intron variant A/G snv 0.38 0.010 1.000 1 2014 2014
CATARACT, ANTERIOR POLAR
CUI: C1855179
Disease: CATARACT, ANTERIOR POLAR
27 0.641 0.480 3 52227015 intron variant A/G snv 0.38 0.010 1.000 1 2016 2016
Chronic gastritis
CUI: C0085695
Disease: Chronic gastritis
11 0.641 0.480 3 52227015 intron variant A/G snv 0.38 0.010 1.000 1 2019 2019
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.641 0.480 3 52227015 intron variant A/G snv 0.38 0.010 1.000 1 2017 2017
Community acquired pneumonia
CUI: C0694549
Disease: Community acquired pneumonia
13 0.641 0.480 3 52227015 intron variant A/G snv 0.38 0.010 1.000 1 2016 2016
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
233 0.641 0.480 3 52227015 intron variant A/G snv 0.38 0.010 1.000 1 2010 2010
Graves Disease
CUI: C0018213
Disease: Graves Disease
252 0.641 0.480 3 52227015 intron variant A/G snv 0.38 0.010 1.000 1 2017 2017
Hepatitis
CUI: C0019158
Disease: Hepatitis
33 0.641 0.480 3 52227015 intron variant A/G snv 0.38 0.010 1.000 1 2018 2018
Hepatitis A
CUI: C0019159
Disease: Hepatitis A
27 0.641 0.480 3 52227015 intron variant A/G snv 0.38 0.010 1.000 1 2018 2018
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
316 0.641 0.480 3 52227015 intron variant A/G snv 0.38 0.010 1.000 1 2014 2014
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
247 0.641 0.480 3 52227015 intron variant A/G snv 0.38 0.010 1.000 1 2016 2016
Liver diseases
CUI: C0023895
Disease: Liver diseases
100 0.641 0.480 3 52227015 intron variant A/G snv 0.38 0.010 1 2019 2019
Malignant neoplasm of endometrium
CUI: C0007103
Disease: Malignant neoplasm of endometrium
197 0.641 0.480 3 52227015 intron variant A/G snv 0.38 0.010 1.000 1 2010 2010
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
289 0.641 0.480 3 52227015 intron variant A/G snv 0.38 0.010 1.000 1 2017 2017
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
448 0.641 0.480 3 52227015 intron variant A/G snv 0.38 0.010 1.000 1 2014 2014
Osteoarthritis of the hand
CUI: C0263746
Disease: Osteoarthritis of the hand
21 0.641 0.480 3 52227015 intron variant A/G snv 0.38 0.010 1.000 1 2019 2019
Osteoarthritis, Knee
CUI: C0409959
Disease: Osteoarthritis, Knee
93 0.641 0.480 3 52227015 intron variant A/G snv 0.38 0.010 1.000 1 2017 2017
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
751 0.641 0.480 3 52227015 intron variant A/G snv 0.38 0.010 1.000 1 2016 2016
Sepsis
CUI: C0243026
Disease: Sepsis
139 0.641 0.480 3 52227015 intron variant A/G snv 0.38 0.010 1.000 1 2011 2011
Septicemia
CUI: C0036690
Disease: Septicemia
139 0.641 0.480 3 52227015 intron variant A/G snv 0.38 0.010 1.000 1 2011 2011
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
392 0.641 0.480 3 52227015 intron variant A/G snv 0.38 0.010 1.000 1 2014 2014
Uterine Cervical Neoplasm
CUI: C0007873
Disease: Uterine Cervical Neoplasm
4 0.641 0.480 3 52227015 intron variant A/G snv 0.38 0.010 1.000 1 2017 2017