rs104894780, DCX

N. diseases: 3
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 0.882 0.120 X 111401121 missense variant G/A snv 0.800 1.000 15 1998 2016
Lissencephaly and agenesis of corpus callosum
CUI: C1848070
Disease: Lissencephaly and agenesis of corpus callosum
11 0.882 0.120 X 111401121 missense variant G/A snv 0.700 0
Malformations of Cortical Development, Group II
CUI: C1837249
Disease: Malformations of Cortical Development, Group II
101 0.882 0.120 X 111401121 missense variant G/A snv 0.700 0