Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2179593
TOX2
0.790 0.080 20 44031646 intron variant C/A snv 0.71 11
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71 25
rs11987193 1.000 0.080 8 29478491 intergenic variant T/C snv 0.71 1
rs12071124
FH
1.000 0.080 1 241520405 upstream gene variant C/A;T snv 0.71 1
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs7130173
C11orf53
1.000 0.080 11 111283347 intron variant A/C snv 0.70 1
rs26279
MSH3
0.790 0.160 5 80873118 missense variant G/A snv 0.73 0.70 9
rs1391441
TET2-AS1 ; TET2
0.763 0.240 4 105207603 intron variant G/A snv 0.70 11
rs9588884 1.000 0.080 13 90145067 intergenic variant C/G snv 0.70 1
rs373572
RAD18
0.882 0.120 3 8913705 missense variant C/T snv 0.68 0.70 6
rs1609682
IL1A
0.882 0.160 2 112782628 intron variant G/T snv 0.70 3
rs639933
C5orf66 ; LOC105379188
0.790 0.080 5 135132061 intron variant C/A snv 0.70 9
rs3783550
IL1A
0.827 0.200 2 112775308 intron variant G/T snv 0.64 0.70 5
rs3787089
RTEL1-TNFRSF6B ; RTEL1
0.790 0.080 20 63685277 intron variant C/T snv 0.70 9
rs4143094
GATA3
0.752 0.240 10 8047173 intron variant T/G snv 0.70 12
rs847208 0.790 0.080 16 86220445 downstream gene variant C/A snv 0.70 9
rs6589219
COLCA2 ; COLCA1
0.790 0.080 11 111302186 intron variant G/C snv 0.69 9
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs7172582
MAP2K5
1.000 0.080 15 67542218 non coding transcript exon variant T/C snv 0.69 1
rs1665650
HSPA12A
0.752 0.160 10 116727589 intron variant T/C snv 0.69 12
rs1862626 0.708 0.280 5 56737113 regulatory region variant G/T snv 0.68 17