Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121908212 0.732 0.160 19 13303877 missense variant G/A snv 14
rs121918799 0.752 0.120 2 166015636 missense variant G/C snv 1.7E-03 1.6E-03 14
rs121908225 0.790 0.120 19 13365448 missense variant G/A snv 12
rs1057520918 0.790 0.160 19 13262780 missense variant C/T snv 11
rs121908217 0.851 0.120 19 13308452 missense variant C/T snv 4.0E-06 9
rs746795369 0.827 0.080 1 160139969 missense variant C/A;T snv 1.2E-05; 4.0E-06 6
rs886037945 0.827 0.160 19 13303584 missense variant C/T snv 6
rs121908211 0.882 0.080 19 13371744 missense variant C/T snv 5
rs121908230 0.882 0.080 19 13262789 missense variant C/T snv 5
rs794727411 0.851 0.160 19 13261526 missense variant C/G;T snv 5
rs121918632 0.851 0.120 2 165996099 missense variant A/G snv 7.0E-06 5
rs121918628 0.851 0.080 2 165998049 missense variant G/T snv 5
rs121908214 0.925 0.080 19 13230185 missense variant T/G snv 4
rs121909324 0.851 0.160 19 13255217 stop gained G/A snv 4
rs121918616 0.882 0.080 1 160130283 missense variant G/A snv 4.0E-06 3
rs28933400 0.882 0.080 1 160135510 missense variant T/C snv 3
rs28933401 0.882 0.120 1 160135246 missense variant G/A snv 3
rs121909326 0.882 0.160 19 13235219 missense variant A/G snv 3
rs121918613 0.925 0.080 1 160128667 missense variant A/G snv 2
rs1553245943 1.000 0.080 1 160137001 missense variant G/A snv 2
rs121908218 0.925 0.080 19 13303576 missense variant G/A;C;T snv 2
rs121908220 0.925 0.120 19 13235685 missense variant G/A snv 2
rs121908223 0.925 0.080 19 13262823 missense variant T/C snv 2
rs121908224 1.000 0.080 19 13235262 missense variant C/T snv 2
rs1402027664 0.925 0.080 19 13312697 missense variant T/C snv 2