Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs28933068 0.645 0.560 4 1805644 missense variant C/A;G;T snv 1.6E-05 30
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
rs28931614 0.672 0.520 4 1804392 missense variant G/A;C snv 21
rs28931615 0.732 0.240 4 1804426 missense variant C/A;T snv 13
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
rs1211533350 0.827 0.120 4 1805638 synonymous variant C/A snv 4.0E-06 7.0E-06 5
rs121913114 0.925 0.120 4 1801930 missense variant A/G;T snv 4.0E-06 2
rs75790268 0.925 0.120 4 1804377 missense variant G/T snv 2