Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs759412116 0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 54
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 48
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 47
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 42
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 42
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 41
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 40
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 38
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 35
rs1884444 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 34
rs9344 0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 30
rs2043211 0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs76763715
GBA
0.658 0.520 1 155235843 missense variant T/C;G snv 2.3E-03 27
rs2227982 0.677 0.480 2 241851281 missense variant G/A snv 9.2E-02 4.3E-02 24
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 23
rs11547328 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 22
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 22
rs1289324472
GBA
0.716 0.400 1 155236354 missense variant T/C snv 1.4E-05 21
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 21