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-02 262
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
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
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
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
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1143634 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs421016
GBA
0.683 0.440 1 155235252 missense variant A/C;G snv 8.0E-06; 1.3E-03 30
rs768623239 0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
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
rs78655421 0.716 0.240 7 117530975 missense variant G/A;C;T snv 1.5E-03; 1.2E-05 18
rs5744168 0.701 0.480 1 223111858 stop gained G/A snv 5.3E-02 4.4E-02 18
rs1800553 0.742 0.240 1 94008251 missense variant C/T snv 4.7E-03 3.0E-03 17
rs213950 0.716 0.320 7 117559479 missense variant G/A snv 0.47 0.57 16