rs142740233, SLC12A5

N. diseases: 3
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, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 14
CUI: C4225245
Disease: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 14
2 0.925 0.080 20 46056217 missense variant G/A;T snv 3.3E-03; 4.0E-06 0.700 1.000 3 2014 2015
Febrile Convulsions
CUI: C0009952
Disease: Febrile Convulsions
65 0.925 0.080 20 46056217 missense variant G/A;T snv 3.3E-03; 4.0E-06 0.010 1.000 1 2014 2014
Idiopathic generalized epilepsy
CUI: C0270850
Disease: Idiopathic generalized epilepsy
24 0.925 0.080 20 46056217 missense variant G/A;T snv 3.3E-03; 4.0E-06 0.010 1.000 1 2014 2014