Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10052957
NR3C1
0.851 0.160 5 143407136 non coding transcript exon variant G/A snv 0.28 4
rs1042114
OPRD1
0.807 0.120 1 28812463 missense variant G/C;T snv 0.91 6
rs1042363
AKAP12
0.882 0.080 6 151356693 3 prime UTR variant T/C snv 4
rs1079597
DRD2
0.827 0.080 11 113425564 intron variant C/T snv 0.18 5
rs1108580
DBH
0.790 0.240 9 133639992 splice region variant A/G snv 0.45 0.54 9
rs111325002 1.000 0.080 3 96134788 intergenic variant A/G snv 8.6E-03 2
rs1126671
ADH4 ; LOC100507053
0.851 0.120 4 99127263 missense variant T/C snv 0.76 0.75 5
rs12071360 1.000 0.080 1 233608833 intergenic variant T/C snv 0.10 1
rs13273442 0.882 0.080 8 42688874 intergenic variant A/G snv 0.66 4
rs1437134
NFAT5
1.000 0.080 16 69696523 3 prime UTR variant A/G snv 0.66 1
rs149775276
CHRNB3
0.925 0.080 8 42732292 missense variant C/T snv 3.6E-04 4.9E-04 2
rs150954431
NCOR2
1.000 0.080 12 124517777 intron variant C/T snv 1.6E-02 2
rs1611115
DBH
0.732 0.280 9 133635393 upstream gene variant T/C snv 0.80 16
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
rs1868152 0.925 0.080 3 186502274 intergenic variant A/G;T snv 0.85 2
rs2005290
OR3A2
1.000 0.080 17 3284718 intron variant C/G;T snv 2
rs2229163
CHRM4
1.000 0.080 11 46385307 synonymous variant G/A snv 1.0E-02 3.9E-02 1
rs2234918
OPRD1
0.827 0.200 1 28863085 synonymous variant C/T snv 0.59 0.50 5
rs2235749
PDYN-AS1 ; PDYN
0.790 0.200 20 1979293 3 prime UTR variant G/A snv 0.37 7
rs2283265
DRD2
0.776 0.160 11 113414814 intron variant C/A snv 0.16 12
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
rs2952621 0.882 0.080 2 129240870 downstream gene variant T/A;C snv 4
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31 23