rs146311723, USP3

N. diseases: 2
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.
Albuminuria
CUI: C0001925
Disease: Albuminuria
59 1.000 0.080 15 63512308 intron variant T/C snv 0.14 0.700 1.000 1 2018 2018
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 1.000 0.080 15 63512308 intron variant T/C snv 0.14 0.700 1.000 1 2018 2018