Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4795541
SLC6A4 ; LOC105371720
0.807 0.200 17 30237299 upstream gene variant A/G snv 7
rs1042114
OPRD1
0.807 0.120 1 28812463 missense variant G/C;T snv 0.91 6
rs684513
CHRNA5
0.925 0.080 15 78566058 intron variant C/G;T snv 5
rs1042363
AKAP12
0.882 0.080 6 151356693 3 prime UTR variant T/C snv 4
rs2952621 0.882 0.080 2 129240870 downstream gene variant T/A;C snv 4
rs2005290
OR3A2
1.000 0.080 17 3284718 intron variant C/G;T snv 2
rs6989250 1.000 0.080 8 53253835 upstream gene variant C/G;T snv 1
rs779838446
CHRNA6
0.925 0.080 8 42756217 missense variant G/A snv 4.0E-06 7.0E-06 2
rs149775276
CHRNB3
0.925 0.080 8 42732292 missense variant C/T snv 3.6E-04 4.9E-04 2
rs111325002 1.000 0.080 3 96134788 intergenic variant A/G snv 8.6E-03 2
rs150954431
NCOR2
1.000 0.080 12 124517777 intron variant C/T snv 1.6E-02 2
rs2229163
CHRM4
1.000 0.080 11 46385307 synonymous variant G/A snv 1.0E-02 3.9E-02 1
rs12071360 1.000 0.080 1 233608833 intergenic variant T/C snv 0.10 1
rs6719226 1.000 0.080 2 25173143 upstream gene variant C/G snv 0.13 1
rs2283265
DRD2
0.776 0.160 11 113414814 intron variant C/A snv 0.16 12
rs1079597
DRD2
0.827 0.080 11 113425564 intron variant C/T snv 0.18 5
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs2629540
FAM53B
0.925 0.080 10 124737579 intron variant G/C snv 0.18 4
rs806368
CNR1
0.752 0.280 6 88140381 3 prime UTR variant T/C snv 0.19 14
rs6871510
HOMER1
1.000 0.080 5 79496521 intron variant C/T snv 0.22 1
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs10052957
NR3C1
0.851 0.160 5 143407136 non coding transcript exon variant G/A snv 0.28 4
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31 23
rs6454674
CNR1
0.851 0.120 6 88163211 intron variant T/G snv 0.32 5