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.
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.925 0.040 19 5851790 intron variant A/G snv 0.76 0.010 1.000 1 2015 2015
GASTRIC CANCER, INTESTINAL
CUI: C3150911
Disease: GASTRIC CANCER, INTESTINAL
3 0.925 0.040 19 5851790 intron variant A/G snv 0.76 0.010 1.000 1 2019 2019
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
385 0.925 0.040 19 5851790 intron variant A/G snv 0.76 0.010 1.000 1 2019 2019
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.925 0.040 19 5851790 intron variant A/G snv 0.76 0.010 1.000 1 2019 2019