Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1557036768 0.708 0.320 X 53647390 missense variant C/T snv 44
rs1563183492 0.708 0.520 7 70766248 missense variant C/T snv 32
rs121908120 0.701 0.280 2 218890289 missense variant T/A snv 1.4E-02 1.4E-02 19
rs147680216 0.742 0.160 2 218890244 missense variant G/A snv 2.1E-03 6.9E-04 11
rs121908119 0.763 0.200 2 218882368 stop gained C/A snv 6.2E-04 8.5E-04 10
rs121908568 0.807 0.160 17 65536495 stop gained G/A snv 9
rs35822372 0.776 0.160 2 88438931 intergenic variant C/A;T snv 8
rs55846652 0.776 0.160 X 69564858 downstream gene variant T/C snv 0.29 8
rs917412 0.776 0.160 4 108350621 TF binding site variant C/T snv 0.21 8
rs2034604 0.776 0.160 2 143201176 intron variant C/G;T snv 8
rs4498834 0.776 0.160 1 201111170 intron variant T/C snv 0.56 8
rs35956082 0.776 0.160 3 71414748 intron variant A/C;G snv 8
rs758468472 0.776 0.160 17 67718094 splice region variant G/T snv 8
rs138249161 0.827 0.240 12 106432421 missense variant T/A snv 2.7E-04 3.0E-04 8
rs730882193 0.807 0.200 17 65536472 stop gained C/G;T snv 6
rs775141057 0.882 0.120 12 106496115 missense variant C/A;T snv 4.0E-06 2.1E-05 6
rs4904210 0.851 0.080 14 36666548 missense variant G/C snv 0.36 0.33 5
rs929387 0.851 0.080 7 41966080 missense variant G/A;C snv 0.43; 5.7E-06 4
rs1553763618 0.925 0.040 1 145977482 splice acceptor variant G/A snv 4
rs782661984 0.925 0.040 1 145974824 splice acceptor variant G/A snv 2.3E-05 1.4E-05 4
rs377467108 0.882 0.120 7 148827254 missense variant C/A;T snv 6.4E-05 3
rs374910216 0.882 0.080 2 218882358 missense variant G/A snv 2.4E-05 3
rs28933971 0.882 0.080 14 36662975 missense variant G/A;C snv 3
rs750190755 0.882 0.080 2 218893087 missense variant C/T snv 4.1E-05 7.0E-06 3
rs1567755946 0.925 0.080 17 65537563 frameshift variant -/CGCGGGAGGCAGC delins 2