rs786205860, KCTD17

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.
DYSTONIA 26, MYOCLONIC
CUI: C4225341
Disease: DYSTONIA 26, MYOCLONIC
1 0.925 0.040 22 37057420 missense variant G/A snv 0.800 0
Myoclonic dystonia
CUI: C1834570
Disease: Myoclonic dystonia
29 0.925 0.040 22 37057420 missense variant G/A snv 0.010 1.000 1 2015 2015