Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7186053
CDH1
1.000 0.080 16 68805390 intron variant A/G snv 0.69 1
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1800624
PBX2 ; AGER
0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 17
rs965513
PTCSC2
0.742 0.200 9 97793827 intron variant A/G;T snv 15
rs3020449
ESR2
0.807 0.200 14 64306674 intron variant A/G;T snv 10
rs3829078
CA9
0.851 0.160 9 35679254 missense variant A/G;T snv 8.2E-02 6
rs438034
CENPF
0.882 0.120 1 214657274 stop gained A/G;T snv 0.61 4
rs1047781
LOC105447645 ; FUT2
0.790 0.200 19 48703374 missense variant A/T snv 3.6E-02 1.2E-02 11
rs11125
LGALS3
0.851 0.120 14 55145121 missense variant A/T snv 6.5E-02 5.7E-02 5
rs3760468
NME1-NME2 ; NME1
0.882 0.120 17 51153130 upstream gene variant A/T snv 0.39 3
rs121913227
BRAF
0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs3816527
PTX3 ; VEPH1
0.882 0.160 3 157437525 missense variant C/A snv 0.64 0.64 9
rs514049
ADAM10
0.827 0.160 15 58750164 intron variant C/A snv 0.57 6
rs767741751
MCPH1 ; ANGPT2
0.851 0.120 8 6562846 missense variant C/A snv 4.0E-06 5
rs2622621
ABCG2
0.851 0.240 4 88109768 intron variant C/A;G snv 6
rs12774070
ADAMTS14
0.925 0.120 10 70753879 missense variant C/A;G snv 0.23 0.19 4
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs3801004
FSCN1
0.882 0.120 7 5598591 intron variant C/A;G;T snv 3
rs10053538
HAVCR2
0.807 0.160 5 157110499 intron variant C/A;T snv 7
rs770327175
CXCR4
0.851 0.120 2 136115878 missense variant C/A;T snv 8.0E-06 5
rs6762208
SENP2
0.851 0.200 3 185613377 missense variant C/A;T snv 0.36; 1.2E-05 4
rs559635697
RHOBTB2
1.000 0.080 8 23007068 missense variant C/A;T snv 2.8E-05 1