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.
Apolipoprotein C-II Deficiency (disorder)
CUI: C1720779
Disease: Apolipoprotein C-II Deficiency (disorder)
5 1.000 0.080 19 44948787 missense variant T/C snv 0.800 1.000 1 1993 1993
apolipoprotein C-II (Wakayama) phenotype
CUI: C4017138
Disease: apolipoprotein C-II (Wakayama) phenotype
1 1.000 0.080 19 44948787 missense variant T/C snv 0.700 0