Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs6265
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.100 0.967 30 2006 2020
dbSNP: rs759834365
rs759834365
BDNF ; BDNF-AS
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.100 1.000 26 2006 2020
dbSNP: rs746682028
rs746682028
BDNF ; BDNF-AS
0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.020 1.000 2 2014 2019
dbSNP: rs11030108
rs11030108
BDNF ; BDNF-AS
1.000 0.040 11 27673917 intron variant A/G snv 0.72
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.010 1.000 1 2013 2013
dbSNP: rs12273363
rs12273363
BDNF
0.807 0.120 11 27723312 intron variant T/C snv 0.16
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.010 1.000 1 2012 2012