Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2069521 0.851 0.240 15 74746626 upstream gene variant G/A snv 4.9E-02 4
rs6785358 0.882 0.200 3 30602723 upstream gene variant G/A snv 0.84 4
rs2278705 0.882 0.160 15 80402288 intron variant C/T snv 4.2E-02 3
rs5915254 0.925 0.120 X 50501281 intergenic variant G/A snv 0.54 2
rs5919436 0.925 0.120 X 67804478 intergenic variant C/G snv 4.0E-02 2
rs6499755 0.925 0.120 16 55307223 intron variant T/C snv 0.30 2
rs7058226 0.925 0.120 X 50483867 intergenic variant G/A snv 0.39 2
rs7063116 0.925 0.120 X 50492002 intergenic variant G/A snv 0.39 2
rs781971826
AKR1C2 ; LOC101928051
1.000 0.120 10 4995793 missense variant C/T snv 4.0E-06 1
rs483352820
AKR1C3
1.000 0.120 10 5102173 missense variant G/A snv 1
rs137852569
AR
0.752 0.320 X 67686030 missense variant G/A snv 9.4E-06 10
rs1020397
ARNT2
0.882 0.160 15 80426396 intron variant G/C;T snv 3
rs5000770
ARNT2
0.882 0.160 15 80424141 intron variant G/A snv 0.27 3
rs1365908231
ATF3
0.925 0.120 1 212619442 missense variant A/C snv 2
rs1377148066
CYP11A1
0.882 0.120 15 74339259 missense variant C/T snv 4.0E-06 7.0E-06 3
rs765057534
CYP19A1 ; MIR4713HG
0.851 0.240 15 51222402 missense variant C/T snv 4.0E-06 4
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs11091748
DGKK
0.925 0.120 X 50414986 intron variant A/G snv 0.39 2
rs12171755
DGKK
0.925 0.120 X 50436751 intron variant C/T snv 0.30 2
rs1934179
DGKK
0.925 0.120 X 50439186 intron variant G/A snv 0.46 2
rs1934190
DGKK
0.925 0.120 X 50400967 intron variant G/A;C snv 0.33 2
rs2211122
DGKK
0.925 0.120 X 50459752 intron variant T/C snv 0.45 2
rs4554617
DGKK
0.925 0.120 X 50460404 intron variant A/C snv 0.45 2
rs4599945
DGKK
0.925 0.120 X 50380968 intron variant G/A;T snv 2
rs4826632
DGKK
0.925 0.120 X 50454263 intron variant G/T snv 0.46 2