rs1264858438, KCNQ2

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.
Benign neonatal epilepsy
CUI: C0270851
Disease: Benign neonatal epilepsy
2 0.925 0.080 20 63406931 missense variant C/T snv 9.0E-06 1.4E-05 0.010 1.000 1 2008 2008
Epilepsy, Rolandic
CUI: C0376532
Disease: Epilepsy, Rolandic
81 0.925 0.080 20 63406931 missense variant C/T snv 9.0E-06 1.4E-05 0.010 1.000 1 2008 2008