rs5997872, SMTN

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 22 31095346 missense variant C/T snv 0.14 0.16 0.010 1.000 1 2012 2012