Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 1
rs1127354 0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 1
rs3743930 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 1
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
rs147001633 0.776 0.240 2 25234373 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 2.2E-04 1
rs387907097 0.925 0.120 20 2417445 missense variant T/G snv 1.5E-04 5.6E-05 1
rs377577594 0.827 0.240 2 25234374 missense variant G/A;C;T snv 1.2E-04; 8.0E-06 1
rs121913502 0.708 0.320 15 90088702 missense variant C/A;T snv 3.2E-05 1
rs371246226 0.827 0.160 21 43094667 missense variant T/C;G snv 2.4E-05; 2.4E-05 1
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 1
rs754921650 1.000 0.040 3 47120446 missense variant T/C snv 1.2E-05 2.1E-05 1
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 1
rs562015640 0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 1
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 1
rs371769427 0.683 0.400 21 43104346 missense variant G/A;T snv 8.0E-06 1
rs1169288572 1.000 0.040 3 47122237 missense variant C/T snv 8.0E-06 7.0E-06 1
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 2
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 2
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 3
rs569067880 0.925 0.080 4 105234864 missense variant G/A;C snv 4.0E-06; 4.0E-06 2
rs1466524306 1.000 0.040 13 99295133 missense variant G/A snv 4.0E-06 1
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 1
rs111033563 0.776 0.240 6 26092916 missense variant A/C snv 4.0E-06 1
rs587780070 0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 1