rs7127507, BDNF-AS;BDNF

N. diseases: 6
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.
Brain atrophy
CUI: C4551584
Disease: Brain atrophy
46 0.827 0.080 11 27693337 intron variant T/C snv 0.34 0.010 1.000 1 2018 2018
Cerebral atrophy
CUI: C0235946
Disease: Cerebral atrophy
44 0.827 0.080 11 27693337 intron variant T/C snv 0.34 0.010 1.000 1 2018 2018
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.827 0.080 11 27693337 intron variant T/C snv 0.34 0.010 1.000 1 2016 2016
Epilepsy, Cryptogenic
CUI: C0086237
Disease: Epilepsy, Cryptogenic
4 0.827 0.080 11 27693337 intron variant T/C snv 0.34 0.010 1.000 1 2016 2016
Memory impairment
CUI: C0233794
Disease: Memory impairment
48 0.827 0.080 11 27693337 intron variant T/C snv 0.34 0.010 1.000 1 2018 2018
Symptomatic epilepsy
CUI: C1406659
Disease: Symptomatic epilepsy
9 0.827 0.080 11 27693337 intron variant T/C snv 0.34 0.010 1.000 1 2016 2016