rs758019788, PREPL

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.
MYASTHENIC SYNDROME, CONGENITAL, 22
CUI: C4479088
Disease: MYASTHENIC SYNDROME, CONGENITAL, 22
9 1.000 2 44338350 splice donor variant C/T snv 3.2E-05 0.700 1.000 1 2014 2014