rs145873257, RBFOX1

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, Rolandic
CUI: C0376532
Disease: Epilepsy, Rolandic
81 1.000 0.040 16 7709117 missense variant G/A;T snv 1.8E-03 0.700 1.000 1 2018 2018