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: rs210987
rs210987
GABRG2
2 0.925 0.080 5 162108749 intron variant C/T snv 0.54 0.010 1.000 1 2016 2016
dbSNP: rs211014
rs211014
GABRG2
2 0.925 0.080 5 162149412 3 prime UTR variant C/A snv 0.30 0.010 1.000 1 2016 2016
dbSNP: rs211037
rs211037
GABRG2
14 0.742 0.240 5 162101274 synonymous variant C/T snv 0.28 0.31 0.010 1.000 1 2016 2016
dbSNP: rs2292096
rs2292096
CAMSAP2
2 0.925 0.040 1 200857641 3 prime UTR variant A/G snv 0.14 0.010 1.000 1 2013 2013
dbSNP: rs2422106
rs2422106
GABRG2
1 1.000 5 162134797 intron variant G/A;T snv 0.010 1.000 1 2016 2016
dbSNP: rs401750
rs401750
GABRG2
2 0.925 0.040 5 162155655 3 prime UTR variant C/T snv 0.43 0.010 1.000 1 2016 2016
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 2016 2016
dbSNP: rs7103411
rs7103411
BDNF ; BDNF-AS
15 0.752 0.160 11 27678578 intron variant C/T snv 0.82 0.010 1.000 1 2016 2016
dbSNP: rs7127507
rs7127507
BDNF ; BDNF-AS
6 0.827 0.080 11 27693337 intron variant T/C snv 0.34 0.010 1.000 1 2016 2016