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: rs1042114
rs1042114
OPRD1
6 0.807 0.120 1 28812463 missense variant G/C;T snv 0.91 0.010 1.000 1 2008 2008
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: rs2234918
rs2234918
OPRD1
5 0.827 0.200 1 28863085 synonymous variant C/T snv 0.59 0.50 0.010 1.000 1 2008 2008
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: rs2952621
rs2952621 		4 0.882 0.080 2 129240870 downstream gene variant T/A;C snv 0.010 1.000 1 2018 2018
dbSNP: rs6713532
rs6713532
POMC
1 1.000 0.080 2 25161964 intron variant T/C snv 0.36 0.010 1.000 1 2009 2009
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: 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: rs1868152
rs1868152 		2 0.925 0.080 3 186502274 intergenic variant A/G;T snv 0.85 0.010 1.000 1 2018 2018
dbSNP: rs1126671
rs1126671
ADH4 ; LOC100507053
5 0.851 0.120 4 99127263 missense variant T/C snv 0.76 0.75 0.010 1.000 1 2005 2005
dbSNP: rs10052957
rs10052957
NR3C1
4 0.851 0.160 5 143407136 non coding transcript exon variant G/A snv 0.28 0.010 1.000 1 2019 2019
dbSNP: rs41423247
rs41423247
NR3C1
23 0.695 0.440 5 143399010 intron variant G/C snv 0.31 0.010 1.000 1 2019 2019
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: 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: rs1042363
rs1042363
AKAP12
4 0.882 0.080 6 151356693 3 prime UTR variant T/C snv 0.010 1.000 1 2005 2005
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: rs13273442
rs13273442 		4 0.882 0.080 8 42688874 intergenic variant A/G snv 0.66 0.010 1.000 1 2014 2014
dbSNP: rs149775276
rs149775276
CHRNB3
2 0.925 0.080 8 42732292 missense variant C/T snv 3.6E-04 4.9E-04 0.010 1.000 1 2014 2014
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: rs1108580
rs1108580
DBH
9 0.790 0.240 9 133639992 splice region variant A/G snv 0.45 0.54 0.010 1.000 1 2010 2010
dbSNP: rs1611115
rs1611115
DBH
16 0.732 0.280 9 133635393 upstream gene variant T/C snv 0.80 0.010 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
dbSNP: rs1079597
rs1079597
DRD2
5 0.827 0.080 11 113425564 intron variant C/T snv 0.18 0.010 1.000 1 2010 2010
dbSNP: rs1800497
rs1800497
ANKK1
56 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 0.010 1.000 1 2010 2010