Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8192917
LOC107984667 ; GZMB
0.925 0.040 14 24632954 missense variant C/T snv 0.76 0.72 3
rs12321603
MDM1 ; LOC105369818
0.882 0.080 12 68293070 intron variant C/T snv 4.4E-02 3
rs3213758
RPGRIP1L
0.925 0.040 16 53605526 missense variant C/T snv 7.3E-02 4.7E-02 3
rs13208776
SMOC2
0.882 0.040 6 168540944 intron variant G/A;C snv 3
rs7758128
TSBP1-AS1
0.882 0.040 6 32377506 intron variant C/A;T snv 4.2E-02 3
rs638893 0.882 0.080 11 118827828 intergenic variant G/A snv 0.79 4
rs7090530 0.851 0.160 10 6068912 downstream gene variant C/A snv 0.59 4
rs997050266
ERCC1
0.851 0.120 19 45423352 missense variant T/A;C snv 1.4E-05 4
rs78645479
FOXD3-AS1 ; FOXD3
0.851 0.120 1 63322631 5 prime UTR variant C/G;T snv 4
rs2456973
LOC105369781 ; IKZF4 ; LOC105369780
0.925 0.040 12 56023144 intron variant A/C;G snv 4
rs11966200
SLC44A4 ; CYP21A2
0.851 0.040 6 31869289 intron variant C/T snv 2.9E-02 4.5E-02 4
rs2269577
XBP1 ; ZNRF3
0.882 0.120 22 28800769 non coding transcript exon variant G/C snv 0.40 4
rs9468925
HLA-B
0.851 0.040 6 31291060 intron variant G/A snv 0.44 5
rs10876864
IKZF4
0.882 0.120 12 56007301 upstream gene variant G/A snv 0.50 5
rs706779
IL2RA
0.827 0.160 10 6056861 intron variant T/C snv 0.48 5
rs4353229
CASP7
0.807 0.160 10 113729830 3 prime UTR variant T/C snv 0.23 6
rs10249788
LOC101927609 ; AHR
0.827 0.160 7 17298523 intron variant C/G;T snv 6
rs2096525
MIF-AS1 ; MIF
0.827 0.280 22 23894632 non coding transcript exon variant T/C snv 0.20 0.20 6
rs1135216
PSMB9 ; TAP1
0.807 0.200 6 32847198 missense variant T/C snv 0.17 0.18 6
rs2257167
IFNAR1
0.807 0.200 21 33343393 missense variant G/C snv 0.18 0.16 7
rs4946936
FOXO3
0.790 0.160 6 108682118 3 prime UTR variant T/A;C snv 8
rs35652124
NFE2L2
0.790 0.320 2 177265345 intron variant T/C snv 0.29 8
rs17587
PSMB9
0.807 0.280 6 32857313 missense variant G/A;T snv 0.24; 4.1E-06; 4.1E-06 8
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 9
rs2294020
CCDC22
0.763 0.280 X 49246763 missense variant A/G;T snv 10