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: rs16969968
rs16969968
CHRNA5
37 0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 0.010 1.000 1 2017 2017
dbSNP: rs1800435
rs1800435
ALAD
7 0.827 0.200 9 113391611 missense variant C/G snv 8.3E-02 6.1E-02 0.010 1.000 1 2018 2018
dbSNP: rs2236861
rs2236861
OPRD1
3 0.882 0.080 1 28813244 intron variant G/A snv 0.19 0.010 1.000 1 2016 2016
dbSNP: rs2722897
rs2722897
PNOC
1 1.000 8 28315680 intron variant A/G snv 0.81 0.010 1.000 1 2016 2016
dbSNP: rs4680
rs4680
COMT ; MIR4761
249 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 0.010 1.000 1 2019 2019