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: rs10411210
rs10411210
RHPN2
13 0.742 0.160 19 33041394 intron variant C/T snv 0.22 0.010 1.000 1 2012 2012
dbSNP: rs10795668
rs10795668
LOC105376400
17 0.724 0.160 10 8659256 upstream gene variant G/A snv 0.24 0.010 1.000 1 2012 2012
dbSNP: rs11174811
rs11174811
AVPR1A
2 1.000 12 63146696 3 prime UTR variant C/A snv 0.12 0.010 1.000 1 2011 2011
dbSNP: rs139994842
rs139994842
NOTCH1
3 0.925 0.040 9 136508308 missense variant G/A;C snv 1.5E-03 0.010 1.000 1 2016 2016
dbSNP: rs1455858
rs1455858
CHRM2 ; LOC349160
3 0.925 0.080 7 136946956 intron variant T/C snv 0.69 0.010 1.000 1 2011 2011
dbSNP: rs16892766
rs16892766 		18 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 0.010 1.000 1 2012 2012
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 2016 2016
dbSNP: rs1799971
rs1799971
OPRM1
95 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 0.010 1.000 1 2017 2017
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 2009 2009
dbSNP: rs279858
rs279858
GABRA2
8 0.851 0.080 4 46312576 synonymous variant T/C snv 0.40 0.38 0.010 1.000 1 2016 2016
dbSNP: rs36021
rs36021
SLC6A2
1 1.000 16 55678038 intron variant T/A snv 0.60 0.010 1.000 1 2016 2016
dbSNP: rs3778150
rs3778150
OPRM1
2 0.925 0.080 6 154062523 intron variant T/C snv 0.17 0.010 1.000 1 2017 2017
dbSNP: rs3802842
rs3802842
COLCA2 ; COLCA1
25 0.695 0.280 11 111300984 intron variant C/A snv 0.71 0.010 1.000 1 2012 2012
dbSNP: rs3811995
rs3811995
GABRA6
1 1.000 5 161685687 intron variant C/T snv 0.48 0.010 1.000 1 2016 2016
dbSNP: rs4444235
rs4444235 		23 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 0.010 1.000 1 2012 2012
dbSNP: rs4779584
rs4779584 		16 0.732 0.160 15 32702555 intergenic variant T/C snv 0.67 0.010 1.000 1 2012 2012
dbSNP: rs4939827
rs4939827
SMAD7
25 0.708 0.160 18 48927093 intron variant T/A;C snv 0.010 1.000 1 2012 2012
dbSNP: rs684513
rs684513
CHRNA5
5 0.925 0.080 15 78566058 intron variant C/G;T snv 0.010 1.000 1 2016 2016
dbSNP: rs6983267
rs6983267
POU5F1B ; CASC8 ; PCAT1 ; CCAT2
62 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 0.010 1.000 1 2012 2012
dbSNP: rs961253
rs961253 		15 0.732 0.240 20 6423634 intergenic variant C/A snv 0.34 0.010 1.000 1 2012 2012
dbSNP: rs9929218
rs9929218
CDH1
16 0.732 0.160 16 68787043 intron variant G/A snv 0.28 0.010 1.000 1 2012 2012