Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519848
EGFR
0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs2279744
MDM2
0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs1057519824
MET
0.807 0.120 7 116783374 missense variant T/G snv 10
rs75790006 0.851 0.040 4 43211547 intron variant T/G snv 1.1E-02 4
rs8178085
PRKDC
0.851 0.080 8 47898144 intron variant T/G snv 2.3E-02 4
rs754626
SRC
0.925 0.080 20 37388937 intron variant T/G snv 0.25 2
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs886039484
TP53
0.641 0.440 17 7674888 missense variant T/C;G snv 32
rs1800975
XPA
0.701 0.360 9 97697296 5 prime UTR variant T/C;G snv 0.63; 4.5E-06; 4.5E-06 19
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs4149056
SLCO1B1
0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs187115
CD44
0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs2229094
LOC100287329 ; LTA
0.776 0.320 6 31572779 missense variant T/C snv 0.27 0.27 17
rs2498801
LOC102723342 ; AKT1
0.790 0.120 14 104769221 upstream gene variant T/C snv 0.41 7
rs1057520018
STK11
0.807 0.080 19 1223124 missense variant T/C snv 6
rs10817938
PTCSC2
0.882 0.080 9 97700127 non coding transcript exon variant T/C snv 3.2E-02 5
rs3087399
REV1
0.882 0.120 2 99438696 missense variant T/C snv 0.13 0.17 4
rs12934561
IL32
0.882 0.080 16 3068864 intron variant T/C snv 0.57 3
rs181696
PLCH1
0.925 0.080 3 155548315 intron variant T/C snv 0.55 3
rs2239815
XBP1
0.925 0.080 22 28796682 non coding transcript exon variant T/C snv 0.44 3
rs4268748
DEF8
0.925 0.080 16 89960104 intron variant T/C snv 0.30 3
rs7309332 1.000 0.040 12 7938243 upstream gene variant T/C snv 0.59 3
rs121913084
FAS
1.000 0.040 10 89010779 missense variant T/C snv 2