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.
Uveitis, Intermediate
CUI: C0042166
Disease: Uveitis, Intermediate
10 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2015 2015
Uveitis
CUI: C0042164
Disease: Uveitis
43 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2015 2015
Urinary tract infection
CUI: C0042029
Disease: Urinary tract infection
14 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2015 2015
Tuberculosis, Pulmonary
CUI: C0041327
Disease: Tuberculosis, Pulmonary
171 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2016 2016
Tuberculosis
CUI: C0041296
Disease: Tuberculosis
328 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.040 1.000 4 2018 2020
Tinnitus
CUI: C0040264
Disease: Tinnitus
14 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2016 2016
Thrombosis of cerebral veins
CUI: C0151945
Disease: Thrombosis of cerebral veins
11 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2015 2015
Takayasu Arteritis
CUI: C0039263
Disease: Takayasu Arteritis
55 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2018 2018
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2012 2012
Stomach Diseases
CUI: C0038354
Disease: Stomach Diseases
3 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2019 2019
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 1.000 2 2012 2014
Steatohepatitis
CUI: C2711227
Disease: Steatohepatitis
75 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2016 2016
Sleep Apnea, Obstructive
CUI: C0520679
Disease: Sleep Apnea, Obstructive
105 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2018 2018
Severe Sepsis
CUI: C1719672
Disease: Severe Sepsis
29 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2015 2015
Septicemia
CUI: C0036690
Disease: Septicemia
141 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2015 2015
Sepsis
CUI: C0243026
Disease: Sepsis
144 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2015 2015
Seizures
CUI: C0036572
Disease: Seizures
553 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2012 2012
Secondary Neoplasm
CUI: C2939419
Disease: Secondary Neoplasm
85 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2017 2017
Secondary malignant neoplasm of colon and/or rectum
CUI: C4721579
Disease: Secondary malignant neoplasm of colon and/or rectum
68 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2016 2016
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.030 1.000 3 2012 2018
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 1.000 2 2017 2018
Rheumatic Heart Disease
CUI: C0035439
Disease: Rheumatic Heart Disease
33 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2016 2016
Retinal Diseases
CUI: C0035309
Disease: Retinal Diseases
56 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2009 2009
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 1.000 2 2014 2015
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.070 0.714 7 2009 2019