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.
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
87 0.878 0.071 2 9956965 intron variant G/T snp 6.0E-02 0.700 1 2016 2016
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
440 0.878 0.071 2 9956965 intron variant G/T snp 6.0E-02 0.700 1 2016 2016
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
760 0.878 0.071 2 9956965 intron variant G/T snp 6.0E-02 0.700 1 2016 2016
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
216 0.878 0.071 2 9956965 intron variant G/T snp 6.0E-02 0.700 1 2016 2016
Heart failure
CUI: C0018801
Disease: Heart failure
91 0.878 0.071 2 9956965 intron variant G/T snp 6.0E-02 0.700 1 2016 2016
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
331 0.878 0.071 2 9956965 intron variant G/T snp 6.0E-02 0.700 1 2016 2016