rs1045642, ABCB1

N. diseases: 214
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 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.100 0.750 32 2005 2018