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: rs1799971
rs1799971
OPRM1
95 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 0.010 1.000 1 2019 2019
dbSNP: rs1824024
rs1824024
CHRM2 ; LOC349160
4 0.851 0.160 7 136958947 intron variant C/A snv 0.65 0.010 1.000 1 2018 2018
dbSNP: rs2229902
rs2229902
GRM7
4 0.851 0.160 3 7452730 missense variant A/T snv 0.31 0.30 0.010 1.000 1 2002 2002
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 2004 2004
dbSNP: rs6276
rs6276
DRD2
8 0.807 0.320 11 113410675 3 prime UTR variant C/T snv 0.54 0.010 1.000 1 2010 2010
dbSNP: rs6691840
rs6691840
GRIK3
5 0.827 0.120 1 36859876 missense variant A/C;G snv 0.27; 9.2E-05 0.010 1.000 1 2006 2006
dbSNP: rs746682028
rs746682028
BDNF ; BDNF-AS
36 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2004 2004
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 2004 2004