Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 26
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs397517201 0.732 0.240 3 179218307 missense variant A/C;G;T snv 16
rs1057519940 0.752 0.200 3 179218308 missense variant G/T snv 13
rs1057519936 0.776 0.200 3 179234284 missense variant A/G;T snv 11
rs1057519937 0.776 0.200 3 179234285 missense variant T/C snv 11
rs121913283 0.724 0.440 3 179234286 missense variant G/A;T snv 4.0E-06 16
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
rs121913399 0.724 0.200 3 41224612 missense variant G/A;C snv 13
rs28931589 0.695 0.240 3 41224613 missense variant G/A;C;T snv 17
rs371769427 0.683 0.400 21 43104346 missense variant G/A;T snv 8.0E-06 24
rs1057519946 0.732 0.280 19 52212729 missense variant C/G;T snv 18
rs1057519947 0.790 0.160 19 52212730 missense variant G/A snv 9
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 37
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 29
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 48
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs1057519874 0.807 0.120 7 6387261 missense variant C/A;T snv 9
rs1057519948 0.851 0.120 7 6387262 missense variant C/T snv 4
rs730882008 0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 23
rs28934574 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 31