Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7765004 0.925 0.120 6 113750518 regulatory region variant A/C snv 0.32 2
rs1390458638
ABCB6
0.925 0.120 2 219216441 missense variant G/A snv 4.0E-06 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
rs1227230819
GDNF ; GDNF-AS1
0.925 0.120 5 37815877 missense variant T/C snv 4.0E-06 2
rs7712513
LOC101927357
0.925 0.120 5 122582513 intergenic variant G/T snv 0.71 2
rs2070770
MS4A1
0.925 0.120 11 60463058 synonymous variant C/T snv 7.1E-02 5.4E-02 2
rs1239470707
PPARG
0.925 0.120 3 12416785 missense variant C/A snv 2
rs111724149
PRDM11
0.925 0.120 11 45204720 missense variant A/G snv 1.8E-03 1.8E-03 2
rs35090414
PRDM11
0.925 0.120 11 45224227 missense variant G/A;T snv 1.5E-04; 8.2E-02 2
rs770027749
XBP1
0.925 0.120 22 28795623 missense variant C/A;G snv 8.0E-06 2
rs1178732315
GBA
0.882 0.240 1 155236381 missense variant A/G snv 1.4E-05 3
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
rs1801195
WRN
0.776 0.240 8 31141764 missense variant G/A;T snv 8.0E-06; 0.45 0.46 8
rs20551
EP300
0.752 0.320 22 41152004 missense variant A/G snv 0.31 0.23 10
rs3758391
SIRT1
0.742 0.480 10 67883584 upstream gene variant T/C snv 0.64 11
rs1057520009
XPO1
0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06 14
rs121913496
LRRC56 ; HRAS
0.724 0.440 11 533873 missense variant C/A;G;T snv 16
rs121913238
KRAS
0.732 0.240 12 25227343 missense variant G/C;T snv 17
rs121913240
KRAS
0.672 0.440 12 25227342 missense variant T/A;C;G snv 24
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 25
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 26
rs17851045
KRAS
0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 27
rs28933406
LRRC56 ; HRAS
0.667 0.480 11 533875 missense variant G/C;T snv 27