Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs752021744
PIK3CB
0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29
rs1057519903
H3-3A
0.683 0.080 1 226064434 missense variant A/T snv 28
rs121913495
GNAS
0.672 0.400 20 58909366 missense variant G/A;T snv 28
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs879253942
TP53
0.677 0.400 17 7673826 missense variant A/G snv 28
rs11547328
CDK4
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 27
rs1799939
RET
0.658 0.280 10 43114671 missense variant G/A;C;T snv 0.21 27
rs121912660
TP53
0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs3783553
IL1A
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs1805007
MC1R
0.695 0.280 16 89919709 missense variant C/A;G;T snv 4.4E-02 25
rs6505162
NSRP1 ; MIR3184 ; MIR423
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs78311289
FGFR3
0.689 0.440 4 1806162 missense variant A/C;G snv 4.0E-06 25
rs876658657
MLH1
0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs121913240
KRAS
0.672 0.440 12 25227342 missense variant T/A;C;G snv 24
rs121913338
BRAF
0.677 0.400 7 140753354 missense variant T/A;C;G snv 24
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs121913503
IDH2
0.689 0.200 15 90088606 missense variant C/A;T snv 23
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv 21
rs17855750
IL27
0.695 0.480 16 28503907 missense variant A/C;T snv 6.4E-02; 4.0E-06 21
rs2066827
GPR19 ; CDKN1B
0.695 0.320 12 12718165 missense variant T/A;C;G snv 1.6E-04; 1.6E-05; 0.26 21
rs730882025
TP53
0.724 0.360 17 7674885 missense variant C/A;G;T snv 21
rs1273593548
PIK3CG
0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs2267437
DESI1 ; XRCC6
0.724 0.320 22 41620695 intron variant C/A;G snv 19