rs9444348, NT5E

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.
Nephrotic Syndrome
CUI: C0027726
Disease: Nephrotic Syndrome
45 6 85465856 intron variant G/A snv 0.43 0.010 1.000 1 2018 2018
Seizures
CUI: C0036572
Disease: Seizures
553 6 85465856 intron variant G/A snv 0.43 0.010 1.000 1 2015 2015