Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs2472297 0.882 0.160 15 74735539 intergenic variant C/T snv 0.16 9
rs4410790
LOC101927609 ; AHR
0.882 0.160 7 17244953 intron variant T/C snv 0.54 9
rs4665972
SNX17
2 27375230 intron variant T/C snv 0.69 9
rs1801239
CUBN
0.827 0.160 10 16877053 missense variant T/C;G snv 8.9E-02; 8.0E-06 8
rs2470893
CYP1A1
0.882 0.160 15 74727108 upstream gene variant C/T snv 0.20 8
rs784257
LOC105372130
1.000 0.080 18 55729968 intron variant T/A;C snv 4
rs10995311
ADO
10 62805174 missense variant C/G snv 0.35 0.31 3
rs702634
ARL15
1.000 0.080 5 53975590 intron variant G/A snv 0.72 3
rs45551835
CUBN
1.000 0.080 10 16890385 missense variant G/A;T snv 1.3E-02; 4.0E-06 3
rs112607182 3 170309619 downstream gene variant C/T snv 5.3E-02 2
rs17158386 7 29765745 regulatory region variant G/A snv 0.19 2
rs2236295
ADO
10 62805132 missense variant G/C;T snv 0.32 2
rs67339103
LRMDA
10 76133928 intron variant G/A;C;T snv 2
rs6535594
NR3C2
4 148211605 intron variant G/A snv 0.54 2
rs146311723
USP3
1.000 0.080 15 63512308 intron variant T/C snv 0.14 2
rs10157710 1 47496019 downstream gene variant C/T snv 0.78 1
rs11264327 1 155122631 downstream gene variant G/A;C;T snv 1
rs12032996 1 33454985 intergenic variant G/A snv 0.12 1
rs12727104 1 171454028 intergenic variant G/A snv 8.3E-02 1
rs13394343 2 85527219 intergenic variant C/A;T snv 1
rs16943246 15 45428399 upstream gene variant G/A snv 0.29 1
rs185291443 2 226120788 intergenic variant C/A;G snv 1
rs35311980 2 228295484 intergenic variant C/T snv 4.9E-05 1