Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs920778
HOTAIR
0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs12934561
IL32
0.882 0.080 16 3068864 intron variant T/C snv 0.57 3
rs181696
PLCH1
0.925 0.080 3 155548315 intron variant T/C snv 0.55 3
rs1460816
BRCA2
1.000 0.040 13 32354271 intron variant G/A snv 0.54 1
rs281432
ICAM1
0.851 0.280 19 10279982 intron variant C/G snv 0.52 12
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs6819385
CHRNA9
0.925 0.080 4 40337557 intron variant A/G snv 0.52 2
rs2494938
LRFN2
0.752 0.240 6 40568389 intron variant G/A snv 0.51 11
rs3660
KRT86 ; KRT81
0.882 0.160 12 52286153 3 prime UTR variant C/G snv 0.51 6
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 12
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs12916300
HERC2
0.742 0.080 15 28165345 intron variant C/T snv 0.50 13
rs6791479 1.000 0.040 3 189487243 intergenic variant T/A snv 0.48 1
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs10759637
SLC31A1 ; CDC26
1.000 0.040 9 113262744 3 prime UTR variant A/C snv 0.47 2
rs602662
LOC105447645 ; FUT2
0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47 16
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs2285947
DNAH11
0.807 0.120 7 21544470 intron variant G/A snv 0.44 7
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs2239815
XBP1
0.925 0.080 22 28796682 non coding transcript exon variant T/C snv 0.44 3
rs454421
KLC3
1.000 0.040 19 45341392 intron variant C/G;T snv 0.44 1
rs7182283
NEIL1
0.925 0.120 15 75351418 intron variant G/T snv 0.43 2
rs2498801
LOC102723342 ; AKT1
0.790 0.120 14 104769221 upstream gene variant T/C snv 0.41 7
rs1047840
EXO1
0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19
rs3732183
MSH2
1.000 0.040 2 47466820 intron variant G/A;T snv 0.34; 4.0E-06 0.40 1