Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 1
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 3
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 3
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 1
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 1
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 1
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 2
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 1
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 4
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 1
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 2
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 2
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 1
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 2
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 1
rs3743930 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 1
rs121913507
KIT
0.614 0.400 4 54733155 missense variant A/T snv 2
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 1
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 2
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 2
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 1
rs1127354 0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 1
rs28933406 0.667 0.480 11 533875 missense variant G/C;T snv 1
rs121913240 0.672 0.440 12 25227342 missense variant T/A;C;G snv 1
rs17851045 0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 1