Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11191580 0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 12
rs796052571 0.851 0.040 12 13608755 missense variant C/T snv 6
rs1057521223 1.000 0.040 2 165373339 stop gained G/A;T snv 5
rs2535629 0.827 0.040 3 52799203 intron variant G/A;C snv 5
rs1568070621 1.000 0.040 17 67918746 frameshift variant AG/- delins 4
rs1057519440 1.000 0.040 X 51744647 missense variant G/A snv 3
rs11585926 1.000 0.040 1 114431068 intron variant T/C snv 0.22 3
rs587777162 0.925 0.040 20 63495972 missense variant C/T snv 3
rs11102800 1.000 0.040 1 114498310 intron variant C/T snv 0.58 2
rs1559619762 1.000 0.040 3 70977827 splice donor variant C/G snv 2
rs4765905 0.827 0.040 12 2240418 intron variant G/A;C snv 2
rs4773054 1.000 0.040 13 109501681 intron variant T/C snv 0.89 2
rs7122539
PC
0.925 0.040 11 66895260 intron variant G/A snv 0.43 2
rs9635542
PPL
1.000 0.040 16 4951379 intron variant A/G snv 0.11 2
rs10038113 1.000 0.040 5 25902233 intergenic variant T/C snv 0.45 1
rs10058083 1.000 0.040 5 25894289 intergenic variant G/A snv 0.38 1
rs10185592 1.000 0.040 2 205829457 intergenic variant A/C snv 0.11 1
rs10205350 1.000 0.040 2 30923631 intron variant G/T snv 0.24 1
rs10239799 1.000 0.040 7 120765281 intergenic variant C/T snv 0.37 1
rs10489525 1.000 0.040 1 114721064 intron variant G/A snv 0.32 1
rs10498676 0.925 0.040 6 11026766 intron variant G/A snv 0.18 1
rs10513025 1.000 0.040 5 9623510 non coding transcript exon variant T/C snv 5.4E-02 1
rs1057518658 1.000 0.040 2 165331409 frameshift variant AC/- del 1
rs1057518993 1.000 0.040 X 53243367 stop gained G/A snv 1
rs1057518999 1.000 0.040 3 70977826 splice donor variant A/G snv 1