rs587783579, 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.
Abnormal cortical gyration
CUI: C1856019
Disease: Abnormal cortical gyration
12 1.000 0.080 X 111401014 frameshift variant T/-;TT delins 0.700 0
Malformations of Cortical Development, Group II
CUI: C1837249
Disease: Malformations of Cortical Development, Group II
101 1.000 0.080 X 111401014 frameshift variant T/-;TT delins 0.700 0