rs10030601, IQCM

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 4 149804060 intron variant T/C snv 0.22 0.800 1.000 1 2012 2012