rs68082256, None

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, Generalized
CUI: C0014548
Disease: Epilepsy, Generalized
36 1.000 0.040 6 16971344 intergenic variant G/A snv 0.17 0.700 1.000 1 2018 2018