rs1898830, TLR2

N. diseases: 10
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.
Congenital cytomegalovirus infection
7 0.807 0.280 4 153687301 intron variant A/G snv 0.30 0.020 1.000 2 2013 2016
Bacterial Vaginosis
CUI: C0085166
Disease: Bacterial Vaginosis
15 0.807 0.280 4 153687301 intron variant A/G snv 0.30 0.010 1.000 1 2012 2012
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.807 0.280 4 153687301 intron variant A/G snv 0.30 0.010 1.000 1 2015 2015
Familial lichen amyloidosis
CUI: C0268398
Disease: Familial lichen amyloidosis
24 0.807 0.280 4 153687301 intron variant A/G snv 0.30 0.010 1.000 1 2013 2013
Hepatitis
CUI: C0019158
Disease: Hepatitis
42 0.807 0.280 4 153687301 intron variant A/G snv 0.30 0.010 1.000 1 2018 2018
Hepatitis A
CUI: C0019159
Disease: Hepatitis A
27 0.807 0.280 4 153687301 intron variant A/G snv 0.30 0.010 1.000 1 2018 2018
Latent Tuberculosis
CUI: C1609538
Disease: Latent Tuberculosis
18 0.807 0.280 4 153687301 intron variant A/G snv 0.30 0.010 1.000 1 2015 2015
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.807 0.280 4 153687301 intron variant A/G snv 0.30 0.010 1 2019 2019
Pelvic Inflammatory Disease
CUI: C0242172
Disease: Pelvic Inflammatory Disease
3 0.807 0.280 4 153687301 intron variant A/G snv 0.30 0.010 1.000 1 2014 2014
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.807 0.280 4 153687301 intron variant A/G snv 0.30 0.010 1 2019 2019