Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2241909
AURKB
0.925 0.080 17 8205021 synonymous variant G/A snv 0.66 0.64 2
rs4711998
IL17A
0.708 0.360 6 52185555 upstream gene variant A/G snv 0.64 16
rs158572
ERCC8 ; NDUFAF2
0.851 0.120 5 60943616 intron variant G/A snv 0.63 4
rs3803662
CASC16
0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 25
rs8126
TNFAIP2
0.807 0.080 14 103137232 3 prime UTR variant C/T snv 0.63 8
rs2612091
ENOSF1
0.882 0.160 18 683607 intron variant C/T snv 0.63 3
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs225359
TFF1
0.882 0.120 21 42367327 upstream gene variant G/A snv 0.62 3
rs2029298
DDB2
0.882 0.080 11 47213167 upstream gene variant C/T snv 0.62 3
rs2230724
JAK2 ; INSL6
0.851 0.120 9 5081780 synonymous variant G/A snv 0.53 0.62 4
rs3743073
CHRNA3
0.807 0.120 15 78617197 intron variant G/T snv 0.61 11
rs2057314
DCBLD1
0.882 0.080 6 117498194 intron variant A/G snv 0.61 3
rs873601
BIVM-ERCC5 ; ERCC5
0.677 0.360 13 102875987 3 prime UTR variant G/A snv 0.59 25
rs1047768
ERCC5 ; BIVM-ERCC5
0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs10434
VEGFA
0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 17
rs3134613
MYCL-AS1 ; MYCL
0.925 0.080 1 39899131 intron variant C/A snv 0.59 2
rs7789045
NOD1
0.925 0.080 7 30454406 intron variant T/A snv 0.59 2
rs2172362
LOC105378667
0.925 0.080 1 39829228 intergenic variant T/C snv 0.58 3
rs326222
DDB2
0.882 0.080 11 47238117 intron variant T/C snv 0.60 0.58 3
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs920778
HOTAIR
0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs1380576
MDM4
0.763 0.240 1 204519150 intron variant G/C snv 0.57 10
rs3807213
IFRD1
0.882 0.200 7 112465699 intron variant G/T snv 0.57 3
rs1713423
TEP1
0.925 0.080 14 20391914 intron variant G/A snv 0.57 2