Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs759252101 1.000 0.080 19 13212143 missense variant C/G snv 4.0E-06 1
rs121908214 0.925 0.080 19 13230185 missense variant T/G snv 4
rs1026872132 1.000 0.080 19 13234934 missense variant T/C snv 7.0E-06 1
rs121909326 0.882 0.160 19 13235219 missense variant A/G snv 3
rs121908224 1.000 0.080 19 13235262 missense variant C/T snv 2
rs121908221 1.000 0.080 19 13235637 missense variant A/G snv 1
rs121908220 0.925 0.120 19 13235685 missense variant G/A snv 2
rs121909324 0.851 0.160 19 13255217 stop gained G/A snv 4
rs121908237 1.000 0.080 19 13259589 missense variant C/A snv 1
rs794727411 0.851 0.160 19 13261526 missense variant C/G;T snv 5
rs121908219 1.000 0.080 19 13261552 missense variant T/C snv 1
rs1057520918 0.790 0.160 19 13262780 missense variant C/T snv 11
rs121908230 0.882 0.080 19 13262789 missense variant C/T snv 5
rs121908223 0.925 0.080 19 13262823 missense variant T/C snv 2
rs768048563 0.925 0.120 19 13298829 missense variant C/T snv 2.6E-05 2
rs121908218 0.925 0.080 19 13303576 missense variant G/A;C;T snv 2
rs121908213 1.000 0.080 19 13303580 missense variant A/G snv 1
rs886037945 0.827 0.160 19 13303584 missense variant C/T snv 6
rs121908212 0.732 0.160 19 13303877 missense variant G/A snv 14
rs121908217 0.851 0.120 19 13308452 missense variant C/T snv 4.0E-06 9
rs1402027664 0.925 0.080 19 13312697 missense variant T/C snv 2
rs886039322 1.000 0.080 19 13312778 missense variant T/C snv 8.9E-06 7.0E-06 2
rs41276886 0.925 0.080 19 13317310 missense variant C/T snv 4.5E-03 4.4E-03 2
rs1555767914 1.000 0.080 19 13335828 missense variant G/A snv 1
rs121908225 0.790 0.120 19 13365448 missense variant G/A snv 12