rs494860, PCID2;PROZ

N. diseases: 1
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.
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 1.000 0.120 13 113164695 intron variant T/A snv 0.26 0.19 0.010 1.000 1 2018 2018