rs1470522542, RELN

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.
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 1.000 0.040 7 103989335 missense variant G/A;C snv 5.0E-06; 5.0E-06 0.010 1.000 1 2011 2011