rs587783191, ARX

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.
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 1
30 0.925 0.160 X 25004894 frameshift variant C/- delins 0.700 0
Lissencephaly, X-Linked, 2
CUI: C1846171
Disease: Lissencephaly, X-Linked, 2
25 0.925 0.160 X 25004894 frameshift variant C/- delins 0.700 0