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: 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: rs3802241
rs3802241
ADRA1A
1 8 26765867 3 prime UTR variant G/A snv 0.55 0.010 1.000 1 2018 2018
dbSNP: rs5574
rs5574
NPY ; LOC107986777
5 0.882 0.200 7 24289514 synonymous variant C/T snv 0.43 0.43 0.010 1.000 1 2018 2018
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: rs77485247
rs77485247
HRH4
3 0.925 0.080 18 24460578 upstream gene variant T/A snv 0.010 1.000 1 2019 2019
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