Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1026872132 1.000 0.080 19 13234934 missense variant T/C snv 7.0E-06 1
rs1057520918 0.790 0.160 19 13262780 missense variant C/T snv 11
rs121908211 0.882 0.080 19 13371744 missense variant C/T snv 5
rs121908212 0.732 0.160 19 13303877 missense variant G/A snv 14
rs121908213 1.000 0.080 19 13303580 missense variant A/G snv 1
rs121908214 0.925 0.080 19 13230185 missense variant T/G snv 4
rs121908217 0.851 0.120 19 13308452 missense variant C/T snv 4.0E-06 9
rs121908218 0.925 0.080 19 13303576 missense variant G/A;C;T snv 2
rs121908219 1.000 0.080 19 13261552 missense variant T/C snv 1
rs121908220 0.925 0.120 19 13235685 missense variant G/A snv 2
rs121908221 1.000 0.080 19 13235637 missense variant A/G snv 1
rs121908222 1.000 0.080 19 13371735 missense variant C/T snv 1
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
rs121908225 0.790 0.120 19 13365448 missense variant G/A snv 12
rs121908230 0.882 0.080 19 13262789 missense variant C/T snv 5
rs121908237 1.000 0.080 19 13259589 missense variant C/A snv 1
rs121909324 0.851 0.160 19 13255217 stop gained G/A snv 4
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
rs121918616 0.882 0.080 1 160130283 missense variant G/A snv 4.0E-06 3
rs121918628 0.851 0.080 2 165998049 missense variant G/T snv 5
rs121918632 0.851 0.120 2 165996099 missense variant A/G snv 7.0E-06 5
rs121918799 0.752 0.120 2 166015636 missense variant G/C snv 1.7E-03 1.6E-03 14
rs1402027664 0.925 0.080 19 13312697 missense variant T/C snv 2