rs587783589, DCX

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.
Lissencephaly, X-Linked, 1
CUI: C4551968
Disease: Lissencephaly, X-Linked, 1
30 0.925 0.080 X 111331042 splice acceptor variant C/T snv 0.700 0
Malformations of Cortical Development, Group II
CUI: C1837249
Disease: Malformations of Cortical Development, Group II
101 0.925 0.080 X 111331042 splice acceptor variant C/T snv 0.700 0