Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 35
rs28934574 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 27
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 25
rs786201057 0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 19
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 16
rs55832599 0.716 0.360 17 7673821 missense variant G/A snv 13
rs1131691003 0.752 0.360 17 7676381 splice donor variant C/A;G snv 12
rs1131691042 0.752 0.360 17 7675052 splice donor variant C/T snv 12