Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 37
rs121913482 0.630 0.680 4 1801837 missense variant C/T snv 35
rs1554888939 0.683 0.640 9 137798823 missense variant G/T snv 58
rs61816761 0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 24
rs387907144 0.716 0.600 6 157181056 stop gained C/A;T snv 34
rs770374710 0.611 0.560 15 23645747 frameshift variant G/-;GG delins 87
rs199469465 0.672 0.560 16 30737343 stop gained C/A;T snv 49
rs28933068 0.645 0.560 4 1805644 missense variant C/A;G;T snv 1.6E-05 17
rs397507545 0.708 0.560 12 112489083 missense variant G/A;C snv 4.0E-06 16
rs267607048 0.752 0.560 10 110964362 missense variant A/G snv 7.0E-06 12
rs114925667 0.672 0.520 3 132675903 missense variant G/A;T snv 1.9E-03; 4.1E-06 62
rs267606826 0.708 0.520 14 28767903 stop gained C/A;G;T snv 38
rs397507520 0.658 0.520 12 112453279 missense variant G/C;T snv 34
rs137854539 0.716 0.520 20 58903703 missense variant C/T snv 27
rs368869806 0.614 0.480 9 95485875 splice acceptor variant C/T snv 4.0E-06 7.0E-06 97
rs752298579 0.701 0.480 22 20061538 missense variant G/A snv 1.4E-04 7.0E-06 48
rs1553770577 0.724 0.480 3 132675342 missense variant T/C snv 37
rs80338796 0.667 0.480 3 12604200 missense variant G/A;C snv 4.0E-06 35
rs1034395178 0.716 0.480 22 20996071 stop gained C/A;T snv 4.0E-06; 8.0E-06 33
rs121918459 0.662 0.440 12 112450368 missense variant A/G snv 1.2E-05 7.0E-06 46
rs867410737 0.708 0.440 19 1242559 missense variant C/T snv 6.7E-06 42
rs387907145 0.695 0.440 16 4800548 stop gained G/A snv 35
rs1060499548 0.724 0.440 9 130872961 missense variant G/A snv 27
rs1064795104 0.790 0.440 2 72498492 stop gained A/C snv 17
rs587777630 0.716 0.440 2 190986921 missense variant G/A snv 15