rs121917722, PEPD

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.
Deficiency of prolidase
CUI: C0268532
Disease: Deficiency of prolidase
12 1.000 0.040 19 33464060 missense variant C/T snv 2.4E-05 0.800 1.000 4 1990 2002