Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913103 0.925 0.080 4 1807262 stop gained A/C;G;T snv 2
rs4647924 0.600 0.520 4 1801844 missense variant C/A;G;T snv 4.2E-06; 4.2E-06 49
rs121913482 0.630 0.680 4 1801837 missense variant C/T snv 45
rs121913483 0.649 0.560 4 1801841 missense variant C/A;G;T snv 4.2E-06; 1.3E-05 31
rs121913105 0.653 0.600 4 1806163 missense variant A/C;T snv 30
rs28933068 0.645 0.560 4 1805644 missense variant C/A;G;T snv 1.6E-05 30
rs78311289 0.689 0.440 4 1806162 missense variant A/C;G snv 4.0E-06 25
rs28931614 0.672 0.520 4 1804392 missense variant G/A;C snv 21
rs121913485 0.716 0.400 4 1804372 missense variant A/G snv 18
rs121913478 0.708 0.640 10 121515280 missense variant T/C snv 17
rs121913479 0.763 0.280 4 1804362 missense variant G/A;T snv 4.0E-06 10
rs121913116 0.763 0.360 4 1799395 missense variant C/T snv 9
rs121913484 0.851 0.240 4 1804365 missense variant A/T snv 5
rs587779383 0.851 0.120 4 1806157 missense variant A/C;G;T snv 5
rs1035549573 0.882 0.120 21 36767227 missense variant C/T snv 8.0E-06 3
rs267606808 0.882 0.120 4 1805396 missense variant A/G snv 3
rs1211533350 0.827 0.120 4 1805638 synonymous variant C/A snv 4.0E-06 7.0E-06 5
rs121913101 0.882 0.080 4 1807260 stop lost T/A;C;G snv 3