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: rs6719226
rs6719226 		1 1.000 0.080 2 25173143 upstream gene variant C/G snv 0.13 0.010 1.000 1 2009 2009
dbSNP: rs678849
rs678849
OPRD1
5 0.882 0.120 1 28818676 intron variant C/T snv 0.44 0.010 1.000 1 2013 2013
dbSNP: rs684513
rs684513
CHRNA5
5 0.925 0.080 15 78566058 intron variant C/G;T snv 0.010 1.000 1 2010 2010
dbSNP: rs6871510
rs6871510
HOMER1
1 1.000 0.080 5 79496521 intron variant C/T snv 0.22 0.010 1.000 1 2005 2005
dbSNP: rs6989250
rs6989250 		1 1.000 0.080 8 53253835 upstream gene variant C/G;T snv 0.010 1.000 1 2013 2013
dbSNP: rs779838446
rs779838446
CHRNA6
2 0.925 0.080 8 42756217 missense variant G/A snv 4.0E-06 7.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs806368
rs806368
CNR1
14 0.752 0.280 6 88140381 3 prime UTR variant T/C snv 0.19 0.010 1.000 1 2009 2009
dbSNP: rs16969968
rs16969968
CHRNA5
37 0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 0.020 1.000 2 2008 2010
dbSNP: rs6454674
rs6454674
CNR1
5 0.851 0.120 6 88163211 intron variant T/G snv 0.32 0.020 1.000 2 2009 2013
dbSNP: rs12071360
rs12071360 		1 1.000 0.080 1 233608833 intergenic variant T/C snv 0.10 0.700 1.000 1 2014 2014
dbSNP: rs111325002
rs111325002 		2 1.000 0.080 3 96134788 intergenic variant A/G snv 8.6E-03 0.800 1.000 1 2014 2014
dbSNP: rs150954431
rs150954431
NCOR2
2 1.000 0.080 12 124517777 intron variant C/T snv 1.6E-02 0.800 1.000 1 2014 2014
dbSNP: rs2005290
rs2005290
OR3A2
2 1.000 0.080 17 3284718 intron variant C/G;T snv 0.800 1.000 1 2014 2014
dbSNP: rs2629540
rs2629540
FAM53B
4 0.925 0.080 10 124737579 intron variant G/C snv 0.18 0.810 1.000 2 2014 2018