Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1000579
STX18-AS1
1.000 0.080 4 4717767 intron variant A/G snv 0.44 3
rs10009145
LOC100507053 ; ADH4
1.000 0.080 4 99126778 intron variant G/A snv 0.39 0.34 1
rs10051667
GABRB2
0.925 0.080 5 161471322 intron variant T/C snv 0.12 2
rs10160548
HTR3A
1.000 0.080 11 113985959 intron variant G/T snv 0.54 1
rs1017418
LOC730100
1.000 0.080 2 51821024 intron variant G/A;C snv 1
rs10196867
CTNNA2
0.925 0.080 2 79751234 intron variant C/G;T snv 5
rs10198241 0.925 0.080 2 226115660 intergenic variant T/C snv 0.58 4
rs10211296
CSRNP3
1.000 0.080 2 165633833 intron variant A/G snv 0.34 3
rs1034866440
AR
0.851 0.160 X 67643401 missense variant G/A snv 5.7E-06 4
rs1034936
CACNA1C
0.882 0.080 12 2551994 intron variant C/T snv 0.61 3
rs1039002
PDE10A
0.851 0.080 6 165741969 intron variant G/A;T snv 5
rs10392
PPP1R16B
0.882 0.160 20 38922292 3 prime UTR variant G/A snv 0.17 6
rs1042114
OPRD1
0.807 0.120 1 28812463 missense variant G/C;T snv 0.91 6
rs1042173
SLC6A4
0.763 0.320 17 30197993 3 prime UTR variant A/C snv 0.40 14
rs1042363
AKAP12
0.882 0.080 6 151356693 3 prime UTR variant T/C snv 4
rs1042364
ADH4 ; LOC100507053
1.000 0.080 4 99124423 stop gained T/A;C snv 0.78 1
rs10483038
KCNJ6
1.000 0.080 21 37652469 intron variant T/C snv 0.26 3
rs10496768
THSD7B
1.000 0.080 2 137322384 intron variant G/A snv 9.5E-02 1
rs10514299
TMEM161B-AS1
0.827 0.120 5 88367793 intron variant C/T snv 0.21 6
rs1051740
EPHX1
0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs1057302
KIAA0040
1.000 0.080 1 175157287 3 prime UTR variant A/G snv 0.38 1
rs1076560
DRD2
0.776 0.120 11 113412966 intron variant C/A snv 0.16 11
rs1079597
DRD2
0.827 0.080 11 113425564 intron variant C/T snv 0.18 5
rs10889635
SGIP1
1.000 0.080 1 66609892 intron variant G/A snv 0.65 1
rs10892169
DSCAML1
1.000 0.080 11 117762339 intron variant A/G snv 0.68 1