Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs634990 0.827 0.040 15 34713872 intergenic variant T/C snv 0.48 6
rs1063147
BLM
0.807 0.120 15 90811275 synonymous variant C/T snv 0.15 6
rs587778872 0.807 0.200 2 208128231 missense variant G/A;C snv 8.0E-06 6
rs143810759 0.851 0.280 13 108210371 missense variant C/T snv 1.6E-04 2.1E-04 6
rs28931605 0.807 0.200 2 208124294 missense variant G/A;T snv 4.2E-06; 1.3E-05 6
rs1339616347
WRN
0.925 0.120 8 31068328 splice donor variant G/T snv 6
rs2725383
WRN
0.807 0.120 8 31075099 intron variant C/G snv 0.76 6
rs4733220
WRN
0.807 0.120 8 31043374 intron variant A/G snv 0.50 6
rs1423415130 0.851 0.120 17 50360241 missense variant G/A snv 7.0E-06 6
rs104893736 0.827 0.040 3 186539566 missense variant C/A snv 5
rs1050829 0.827 0.160 X 154535277 missense variant T/A;C snv 1.7E-04; 2.6E-02 5
rs79121622 0.827 0.080 16 67165833 missense variant G/A snv 3.3E-04 9.8E-05 5
rs387907338 0.827 0.200 11 111911559 missense variant G/A;T snv 5
rs8702 0.851 0.160 14 103686015 3 prime UTR variant C/G snv 0.61 5
rs80338829 0.851 0.200 22 36295069 missense variant G/A snv 5
rs6841698 0.882 0.080 4 38760093 upstream gene variant G/A snv 0.36 4
rs1303044966 0.882 0.160 20 25339294 stop gained G/A;C snv 4.0E-06 4
rs8027411 0.882 0.040 15 79168687 intron variant G/T snv 0.52 4
rs765919785 0.882 0.080 21 45477409 splice acceptor variant A/G snv 8.2E-06 2.8E-05 4
rs141638421 0.882 0.080 11 111908822 missense variant C/T snv 7.2E-05 4.9E-05 4
rs387907339 0.882 0.280 11 111908967 missense variant C/A;G snv 4
rs150857132 0.851 0.200 2 208124183 missense variant C/A;T snv 4.4E-04; 4.0E-06 4
rs1114167307 0.851 0.200 13 20143233 missense variant G/A snv 4
rs137853924 0.851 0.200 2 208128343 missense variant C/A;T snv 4
rs398122944 0.851 0.200 2 208128257 stop gained C/G;T snv 4