rs2292096, CAMSAP2

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.
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.925 0.040 1 200857641 3 prime UTR variant A/G snv 0.14 0.810 1.000 2 2012 2013
Symptomatic epilepsy
CUI: C1406659
Disease: Symptomatic epilepsy
9 0.925 0.040 1 200857641 3 prime UTR variant A/G snv 0.14 0.010 1.000 1 2013 2013