rs1555491648, GRIN2A

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, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION
CUI: C3806402
Disease: EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT MENTAL RETARDATION
38 0.925 0.040 16 9822337 missense variant G/A snv 0.700 1.000 12 2010 2017
Epilepsy, Rolandic
CUI: C0376532
Disease: Epilepsy, Rolandic
81 0.925 0.040 16 9822337 missense variant G/A snv 0.700 1.000 1 2018 2018