Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs2266788 0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 19
rs1129844 0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05 13
rs5065 0.763 0.240 1 11846011 stop lost A/G snv 0.14 0.21 12
rs10811656 0.807 0.200 9 22124473 intron variant C/T snv 0.47 7
rs376307381 0.925 0.080 11 44067827 missense variant G/C snv 4.0E-06 2