Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1332099 0.724 0.240 10 99538694 downstream gene variant T/C;G snv 14
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs11190133 0.827 0.120 10 99518968 intergenic variant C/T snv 0.26 5
rs9554587 0.827 0.120 13 99388400 downstream gene variant A/G snv 0.17 5
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs9513593
GPR183 ; UBAC2
1.000 0.040 13 99298006 intron variant G/A snv 0.71 1
rs9297145
KPNA7
0.827 0.120 7 99161494 intergenic variant C/A snv 0.67 6
rs142903734
LOC107987207
1.000 0.040 14 98202442 intron variant GA/-;GAGA delins 1
rs6056869
PAK5
1.000 0.040 20 9781800 intron variant G/A;C snv 1
rs2303138
LNPEP
1.000 0.040 5 97015006 missense variant G/A snv 0.13 9.4E-02 1
rs2910686
ERAP2 ; ERAP1
0.827 0.120 5 96916885 intron variant T/C snv 0.42 5
rs4869313
ERAP2 ; ERAP1
0.724 0.240 5 96888176 intron variant T/A;G snv 14
rs2549803
ERAP1
0.827 0.120 5 96839226 intron variant C/T snv 0.27 5
rs151823
ERAP1
1.000 0.040 5 96824289 intron variant A/C snv 0.90 1
rs26653
ERAP1
0.882 0.080 5 96803547 missense variant C/A;G;T snv 0.64; 8.0E-06; 9.1E-04 4
rs30187
ERAP1
0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 14
rs469758
LOC102724748 ; ERAP1
0.827 0.120 5 96786011 intron variant C/T snv 0.62 0.63 5
rs39841
LOC102724748 ; ERAP1
1.000 0.040 5 96784466 intron variant G/A;C snv 1
rs27432
ERAP1 ; LOC102724748
0.925 0.040 5 96783569 intron variant A/C;G snv 2
rs27044
ERAP1 ; LOC102724748
0.827 0.240 5 96783148 missense variant G/C snv 0.69 0.71 5
rs27524
ERAP1 ; CAST
0.851 0.160 5 96766240 intron variant A/G snv 0.61 4
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs2497318 0.827 0.120 10 92672243 upstream gene variant C/A;T snv 6
rs2666218
ASAP2
0.827 0.120 2 9262859 intron variant A/G snv 0.32 5