Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs773442580
EGF
0.851 0.080 4 109913367 missense variant T/C;G snv 4.0E-06 7
rs1476157710
WNT10B
0.925 0.040 12 48970460 missense variant T/C snv 4.1E-06 1.4E-05 3
rs766727892
TCF7L2
0.925 0.040 10 113151107 missense variant G/A snv 1.2E-05 7.0E-06 3
rs867657798
TCF4
0.925 0.040 18 55631366 missense variant G/A;C snv 1.4E-05 3
rs137852972
BSCL2 ; HNRNPUL2-BSCL2
0.752 0.240 11 62702499 missense variant T/C snv 1.6E-05 10
rs371409680
TP53
0.790 0.120 17 7673772 missense variant C/G;T snv 4.0E-05 7.0E-06 10
rs118101777
IDH2
0.614 0.280 15 90087472 missense variant C/T snv 2.0E-03 1.6E-03 42
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs3745601
P2RY11 ; PPAN-P2RY11
0.882 0.120 19 10113872 missense variant G/A snv 0.16 0.13 3
rs1801275
IL4R
0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157