Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 73
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 48
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 42
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 35
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 34
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 29
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 21
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 21
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 19
rs56084662
FRY
0.701 0.280 13 32295727 3 prime UTR variant G/A snv 3.5E-03 18
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 18
rs10936599 0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 18
rs483352697 0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 18
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 18
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 17
rs75316749 0.701 0.280 3 169043635 intergenic variant A/G snv 4.2E-02 17
rs78378222 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 17
rs4246215 0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 16
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 16
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 16
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 15
rs174548 0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 15