Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801275
IL4R
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs121913499
IDH1
0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs28934578
TP53
0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs118101777
IDH2
0.614 0.280 15 90087472 missense variant C/T snv 2.0E-03 1.6E-03 42
rs55819519
TP53
0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04 40
rs1444669684
CDKN2B-AS1 ; CDKN2A
0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs1982073
TGFB1
0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs1057519903
H3-3A
0.683 0.080 1 226064434 missense variant A/T snv 28
rs121912660
TP53
0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs121909218
PTEN
0.672 0.360 10 87933145 missense variant G/A snv 25
rs121913503
IDH2
0.689 0.200 15 90088606 missense variant C/A;T snv 23
rs1805015
IL4R
0.683 0.520 16 27362859 missense variant T/C snv 0.16 0.22 22
rs1273593548
PIK3CG
0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs4644
LGALS3
0.732 0.320 14 55138217 missense variant C/A;G snv 0.35 14
rs4652
LGALS3
0.752 0.200 14 55138318 missense variant A/C snv 4.1E-06; 0.45 0.57 12
rs74315452
SOD1
0.732 0.160 21 31667356 missense variant T/C snv 12
rs6971
TSPO
0.742 0.200 22 43162920 missense variant A/G snv 0.76 0.75 11
rs371409680
TP53
0.790 0.120 17 7673772 missense variant C/G;T snv 4.0E-05 7.0E-06 10
rs76151636
ATP7B
0.776 0.280 13 51944145 missense variant G/A;T snv 4.0E-06; 9.2E-04 10
rs2904551
PRODH
0.776 0.160 22 18918421 missense variant A/G snv 5.2E-03 2.8E-03 8
rs149840192
EGFR
0.807 0.080 7 55154129 missense variant C/A;T snv 7
rs753152604
CDK4
0.827 0.040 12 57751680 missense variant C/A snv 7
rs769809364
TP73
0.807 0.080 1 3732940 missense variant G/A snv 8.5E-06 1.4E-05 7