rs10462087, HCN1

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.
Absence Epilepsy
CUI: C0014553
Disease: Absence Epilepsy
17 0.925 0.040 5 45295178 intron variant T/C snv 5.5E-02 0.010 1.000 1 2018 2018
Childhood Absence Epilepsy
CUI: C4281785
Disease: Childhood Absence Epilepsy
13 0.925 0.040 5 45295178 intron variant T/C snv 5.5E-02 0.010 1.000 1 2018 2018