Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2738780
RTEL1-TNFRSF6B ; RTEL1
0.882 0.080 20 63668461 intron variant T/C snv 0.99 3
rs842226
MUC4
0.882 0.080 3 195751990 non coding transcript exon variant A/G snv 0.95 3
rs4759314
HOTAIR
0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs2267029
MMP11
0.882 0.080 22 23775729 intron variant A/G snv 0.92 3
rs4978754
ELP1
0.851 0.080 9 108884801 intron variant T/C snv 0.92 4
rs9915936
AXIN2
0.827 0.120 17 65537671 synonymous variant T/C snv 0.90 0.90 5
rs2043449
CYP20A1
0.882 0.080 2 203251967 missense variant C/T snv 0.94 0.89 3
rs2025811
XRN2
0.882 0.080 20 21354475 intron variant T/C snv 0.89 3
rs3866958
B9D1 ; MAPK7
0.882 0.080 17 19377693 intron variant A/C;T snv 0.89 3
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs629367
MIR100HG ; MIRLET7A2
0.776 0.200 11 122146306 intron variant C/A snv 0.88 11
rs2230229
TNFRSF10A
0.807 0.120 8 23191779 missense variant C/T snv 0.88 0.86 8
rs2929973
CCN4
0.851 0.200 8 133230265 3 prime UTR variant G/T snv 0.85 5
rs5883064
HOTTIP
0.882 0.080 7 27202260 non coding transcript exon variant CT/- delins 0.85 3
rs1047972
AURKA
0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
rs842461
MUC4
0.882 0.080 3 195808743 intron variant G/T snv 0.84 3
rs132770
DESI1 ; XRCC6
0.752 0.320 22 41621260 5 prime UTR variant A/G snv 0.83 14
rs3096337
MUC4
0.882 0.080 3 195806461 intron variant C/T snv 0.82 3
rs2158041
AHR
0.807 0.160 7 17328796 intron variant T/C snv 0.81 6
rs336958
HAPLN1
0.882 0.080 5 83677577 intron variant T/C snv 0.81 3
rs151606
FGFR1OP
0.882 0.080 6 167016994 intron variant T/A snv 0.81 3
rs465646
REV3L ; MFSD4B
0.882 0.080 6 111299555 3 prime UTR variant G/A snv 0.80 3
rs3131837
RTCA-AS1
0.882 0.080 1 100252204 non coding transcript exon variant C/G snv 0.80 3
rs2057482
HIF1A-AS2 ; HIF1A-AS3 ; HIF1A
0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs738792
MMP11
0.827 0.240 22 23779191 missense variant C/T snv 0.84 0.80 6