rs1318653, MIR29B2CHG

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.
Febrile Convulsions
CUI: C0009952
Disease: Febrile Convulsions
65 1.000 0.080 1 207841577 intron variant T/C snv 0.19 0.710 1.000 1 2014 2014