rs121909508, CHRND

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, 3B, FAST-CHANNEL
CUI: C4225371
Disease: MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL
5 1.000 2 232526664 missense variant T/C snv 0.700 0