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.
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 0.010 1.000 1 2017 2017
Oral Cavity Carcinoma
CUI: C0151546
Disease: Oral Cavity Carcinoma
16 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 0.010 1.000 1 2017 2017
Osteitis Deformans
CUI: C0029401
Disease: Osteitis Deformans
58 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 0.010 1.000 1 2015 2015
Paratuberculosis
CUI: C0030524
Disease: Paratuberculosis
6 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 0.010 1.000 1 2014 2014
Pediatric Crohn's disease
CUI: C2931133
Disease: Pediatric Crohn's disease
6 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 0.010 1.000 1 2013 2013
Pharyngeal Carcinoma
CUI: C0747548
Disease: Pharyngeal Carcinoma
7 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 0.010 1.000 1 2017 2017
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 0.010 1.000 1 2017 2017
Recurrent urinary tract infection
CUI: C0262655
Disease: Recurrent urinary tract infection
21 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 0.010 1.000 1 2019 2019
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 0.010 1.000 1 2016 2016
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 0.010 1.000 1 2016 2016
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 0.010 1.000 1 2016 2016
Urinary tract infection
CUI: C0042029
Disease: Urinary tract infection
14 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 0.010 1.000 1 2019 2019