Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs180414
SLC38A4
0.882 0.080 12 46775115 synonymous variant A/G snv 3.1E-03 3
rs7037324
LOC112268051
0.882 0.080 9 97896036 regulatory region variant A/G snv 0.71 3
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1136201
ERBB2
0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs965513
PTCSC2
0.742 0.200 9 97793827 intron variant A/G;T snv 15
rs397517132
EGFR
0.623 0.280 7 55191846 missense variant A/T snv 48
rs1418810723
FN1
0.851 0.080 2 215409981 missense variant A/T snv 8.0E-06 9
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs2145418 0.882 0.080 1 118422631 intergenic variant C/A snv 0.78 3
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs3219489
MUTYH
0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27 24
rs104894228
LRRC56 ; HRAS
0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs778212685
CHEK2
0.827 0.120 22 28712015 missense variant C/A;G;T snv 4.0E-06 8
rs768891111
XRCC3 ; KLC1
0.851 0.080 14 103699474 stop gained C/A;G;T snv 4.0E-06; 4.0E-06 4
rs747463591
CCDC6
0.882 0.080 10 59906391 missense variant C/A;G;T snv 4.9E-06; 9.9E-06 3
rs78929565
CLOCK
0.882 0.080 4 55539035 intron variant C/A;T snv 3
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs25489
XRCC1
0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs966423
DIRC3
0.776 0.200 2 217445617 intron variant C/G;T snv 11
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs944289 0.742 0.200 14 36180040 upstream gene variant C/T snv 0.45 16
rs2221903
IL21-AS1 ; IL21
0.752 0.360 4 122617757 intron variant C/T snv 0.77 12
rs116909374 0.776 0.120 14 36269155 regulatory region variant C/T snv 2.3E-02 11
rs12508721
IL21-AS1
0.742 0.360 4 122623509 intron variant C/T snv 0.24 11