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.
AURAL ATRESIA, CONGENITAL
CUI: C1842937
Disease: AURAL ATRESIA, CONGENITAL
29 0.882 0.160 3 151371438 intron variant C/G;T snv 0.010 1.000 1 2019 2019
Coronary Aneurysm
CUI: C0010051
Disease: Coronary Aneurysm
17 0.882 0.160 3 151371438 intron variant C/G;T snv 0.010 1.000 1 2019 2019
Mucocutaneous Lymph Node Syndrome
CUI: C0026691
Disease: Mucocutaneous Lymph Node Syndrome
195 0.882 0.160 3 151371438 intron variant C/G;T snv 0.010 1.000 1 2019 2019