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 0.020 1.000 2 2013 2018
dbSNP: rs1045642
rs1045642
ABCB1
214 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2012 2012
dbSNP: rs16979956
rs16979956
BMX ; ACE2
2 X 15525068 intron variant C/T snv 4.0E-04 0.010 1.000 1 2014 2014
dbSNP: rs2032582
rs2032582
ABCB1
97 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2012 2012
dbSNP: rs2304297
rs2304297
CHRNA6
2 8 42753056 3 prime UTR variant G/C snv 0.39 0.010 1.000 1 2014 2014
dbSNP: rs34637584
rs34637584
LRRK2
78 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 0.010 1.000 1 2018 2018
dbSNP: rs35697037
rs35697037
BMX ; ACE2
2 X 15523993 intron variant G/A snv 0.37 0.010 1.000 1 2014 2014
dbSNP: rs3743077
rs3743077
CHRNA3
3 1.000 0.040 15 78602554 intron variant C/T snv 0.31 0.010 1.000 1 2014 2014
dbSNP: rs7136446
rs7136446
IGF1 ; LINC02456
8 0.882 0.160 12 102444737 intron variant C/T snv 0.66 0.010 1.000 1 2019 2019
dbSNP: rs7178176
rs7178176
CHRNA7
2 15 32151612 intron variant C/T snv 0.18 0.010 1.000 1 2014 2014
dbSNP: rs755204
rs755204
CHRNA4 ; LOC100130587
2 20 63362813 intron variant G/A snv 8.6E-02 0.010 1.000 1 2014 2014
dbSNP: rs7812298
rs7812298
CHRNA6
2 8 42753436 intron variant C/T snv 0.36 0.010 1.000 1 2014 2014
dbSNP: rs7828365
rs7828365
CHRNA6
2 8 42774171 intron variant C/T snv 0.14 0.010 1.000 1 2014 2014
dbSNP: rs972936
rs972936
IGF1 ; LINC02456
12 0.807 0.200 12 102431143 intron variant T/C snv 0.70 0.010 1.000 1 2019 2019