Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11644461
rs11644461
GRIN2A
1 1.000 0.080 16 10027033 intron variant T/C snv 0.34 0.010 1.000 1 2012 2012
dbSNP: rs6265
rs6265
BDNF ; BDNF-AS
272 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2012 2012
dbSNP: rs7192557
rs7192557
GRIN2A
1 1.000 0.080 16 10029612 intron variant G/A;T snv 0.21 0.010 1.000 1 2012 2012
dbSNP: rs988748
rs988748
BDNF
3 0.882 0.120 11 27703198 intron variant C/G snv 0.83 0.010 1.000 1 2012 2012