rs141191660, KCTD7

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.
Myoclonic Epilepsies, Progressive
CUI: C0751778
Disease: Myoclonic Epilepsies, Progressive
17 1.000 0.040 7 66639189 missense variant A/G snv 1.2E-05 7.0E-06 0.010 1.000 1 2016 2016