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: rs1017412
rs1017412
NTRK3
1 1.000 0.040 15 87868912 3 prime UTR variant G/A;C snv 0.010 1.000 1 2008 2008
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 2011 2011
dbSNP: rs7176429
rs7176429
NTRK3
1 1.000 0.040 15 87876193 3 prime UTR variant T/A;G snv 0.010 1.000 1 2008 2008
dbSNP: rs759834365
rs759834365
BDNF ; BDNF-AS
237 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 0.010 1.000 1 2011 2011