Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs113993959 0.677 0.280 7 117587778 stop gained G/A;T snv 8.0E-06; 3.4E-04 25
rs5743618 0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 25
rs2227306 0.677 0.680 4 73741338 intron variant C/T snv 0.31 21
rs74597325 0.708 0.320 7 117587811 stop gained C/G;T snv 6.8E-05 18
rs213950 0.716 0.320 7 117559479 missense variant G/A snv 0.47 0.57 16
rs75527207 0.732 0.440 7 117587806 missense variant G/A snv 1.8E-04 3.0E-04 15
rs721917 0.752 0.360 10 79946568 missense variant A/G snv 0.47 0.42 14
rs77010898 0.742 0.280 7 117642566 stop gained G/A;C snv 4.6E-04; 4.0E-06 13
rs1124 0.882 0.160 8 22164004 missense variant G/A snv 0.30 0.26 3
rs121908755 0.882 0.200 7 117587800 missense variant G/A;T snv 8.8E-05 3