Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs1800797
IL6 ; IL6-AS1 ; STEAP1B
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs1057519695
NRAS
0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs1057519834
NRAS
0.658 0.480 1 114713908 missense variant TG/CT mnv 31
rs121913254
NRAS
0.658 0.440 1 114713909 stop gained G/A;C;T snv 31
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs28933406
LRRC56 ; HRAS
0.667 0.480 11 533875 missense variant G/C;T snv 27
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 26
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 25
rs121913240
KRAS
0.672 0.440 12 25227342 missense variant T/A;C;G snv 24
rs121913238
KRAS
0.732 0.240 12 25227343 missense variant G/C;T snv 17
rs121913496
LRRC56 ; HRAS
0.724 0.440 11 533873 missense variant C/A;G;T snv 16
rs3758391
SIRT1
0.742 0.480 10 67883584 upstream gene variant T/C snv 0.64 11
rs10484561 0.827 0.160 6 32697643 intergenic variant T/G snv 0.13 6
rs6449182
CD38
0.807 0.160 4 15778830 intron variant C/G snv 0.22 6
rs1178732315
GBA
0.882 0.240 1 155236381 missense variant A/G snv 1.4E-05 3
rs1239470707
PPARG
0.925 0.120 3 12416785 missense variant C/A snv 2
rs1312391542
ATG5 ; PRDM1
0.925 0.120 6 106104897 missense variant G/A;T snv 2
rs1880030
BCL7A
0.925 0.120 12 122046634 intron variant G/A snv 0.39 2
rs7712513
LOC101927357
0.925 0.120 5 122582513 intergenic variant G/T snv 0.71 2
rs7765004 0.925 0.120 6 113750518 regulatory region variant A/C snv 0.32 2
rs1227230819
GDNF ; GDNF-AS1
0.925 0.120 5 37815877 missense variant T/C snv 4.0E-06 2