Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs753317536
EVC
0.790 0.160 4 5719239 intron variant G/A;C snv 8.0E-06; 4.0E-06 12
rs137852832 0.716 0.280 12 88077263 stop gained C/A snv 9.5E-05 6.3E-05 17
rs121908425 0.763 0.160 4 5748226 stop gained C/A;T snv 3.2E-05; 1.2E-05 14
rs121918327 0.776 0.240 4 122742955 stop gained C/T snv 2.8E-05 1.4E-05 12
rs121908175 0.790 0.160 16 56519791 stop gained G/C snv 5.2E-05 2.8E-05 8
rs147030232 0.827 0.160 16 56501014 stop gained G/A;C snv 2.0E-05; 4.0E-06 8
rs201037487 0.925 0.120 19 38407003 stop gained C/G;T snv 4.0E-06; 1.4E-04; 4.0E-06 4.9E-05 7
rs1553794304 0.851 0.160 3 196707860 stop gained -/T delins 6
rs200750564 0.827 0.160 2 176094518 stop gained C/T snv 8.0E-06 7.0E-06 6
rs886039802 0.851 0.200 15 72712259 stop gained C/T snv 6
rs749974697 0.851 0.240 7 33152851 stop gained C/A;T snv 4.0E-06; 1.6E-05 5
rs775081992 0.851 0.240 7 33152811 stop gained C/T snv 2.0E-05 5
rs786205508 0.851 0.200 17 58208542 stop gained G/A snv 5
rs769975073 0.882 0.120 2 43794508 stop gained G/A snv 6.0E-05 7.0E-06 4
rs879255655 0.882 0.120 2 43809711 stop gained G/T snv 4
rs113624356 0.724 0.400 11 66526181 missense variant T/G snv 1.5E-03 2.1E-03 17
rs879255280
SMO
0.701 0.200 7 129206557 missense variant C/T snv 15
rs886039797 0.807 0.280 16 56502807 missense variant A/C snv 4.0E-06 7
rs751375244 0.827 0.280 1 36139776 missense variant G/A snv 1.2E-05 3.5E-05 6
rs886039811 0.807 0.320 17 19357875 missense variant A/G snv 4.0E-06 6
rs137853105 0.882 0.160 17 58206479 missense variant A/C snv 5.6E-05 2.8E-05 4
rs201948500 0.882 0.120 2 43794485 missense variant C/G snv 2.4E-05 4.9E-05 4
rs281875322 0.807 0.480 18 51078306 missense variant A/G snv 4.0E-06 4
rs118203918 0.882 0.160 6 53016099 missense variant C/T snv 4.0E-06 1
rs121912765 0.925 0.240 14 53951945 missense variant T/C snv 2.4E-05 7.0E-06 1