rs3027898, IRAK1

N. diseases: 11
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.
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
676 0.752 0.360 X 154010439 downstream gene variant C/A snv 0.040 0.500 4 2010 2018
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
213 0.752 0.360 X 154010439 downstream gene variant C/A snv 0.020 1.000 2 2015 2019
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
273 0.752 0.360 X 154010439 downstream gene variant C/A snv 0.010 1.000 1 2010 2010
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.752 0.360 X 154010439 downstream gene variant C/A snv 0.010 1.000 1 2008 2008
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1022 0.752 0.360 X 154010439 downstream gene variant C/A snv 0.010 1 2017 2017
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
635 0.752 0.360 X 154010439 downstream gene variant C/A snv 0.010 1.000 1 2013 2013
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
448 0.752 0.360 X 154010439 downstream gene variant C/A snv 0.010 1.000 1 2019 2019
Oral Ulcer
CUI: C0149745
Disease: Oral Ulcer
7 0.752 0.360 X 154010439 downstream gene variant C/A snv 0.010 1.000 1 2013 2013
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
193 0.752 0.360 X 154010439 downstream gene variant C/A snv 0.010 1.000 1 2020 2020
Subarachnoid Hemorrhage
CUI: C0038525
Disease: Subarachnoid Hemorrhage
26 0.752 0.360 X 154010439 downstream gene variant C/A snv 0.010 1.000 1 2008 2008
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
157 0.752 0.360 X 154010439 downstream gene variant C/A snv 0.010 1 2018 2018