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.
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.882 0.200 5 149428827 intron variant G/A snv 0.12 0.010 1.000 1 2014 2014
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.882 0.200 5 149428827 intron variant G/A snv 0.12 0.010 1.000 1 2016 2016
Congenital heart disease
CUI: C0152021
Disease: Congenital heart disease
80 0.882 0.200 5 149428827 intron variant G/A snv 0.12 0.010 1.000 1 2014 2014
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.882 0.200 5 149428827 intron variant G/A snv 0.12 0.010 1.000 1 2014 2014
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.882 0.200 5 149428827 intron variant G/A snv 0.12 0.010 1.000 1 2019 2019
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.882 0.200 5 149428827 intron variant G/A snv 0.12 0.010 1.000 1 2013 2013
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.882 0.200 5 149428827 intron variant G/A snv 0.12 0.010 1.000 1 2013 2013