Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs199473128 1.000 0.120 3 38603867 stop gained C/A;T snv 8.0E-05 4.9E-05 1
rs137854609 0.882 0.120 3 38581170 missense variant C/A;T snv 7.9E-05 2
rs45465995 1.000 0.120 3 38550683 missense variant G/A snv 7.6E-05; 8.0E-06 9.1E-05 1
rs41311087 0.925 0.120 3 38633255 missense variant C/T snv 7.2E-05 4.2E-05 2
rs199473180 1.000 0.080 3 38581266 missense variant G/A;C snv 6.5E-05 1
rs137854603 1.000 0.080 3 38550602 missense variant C/T snv 6.0E-05 2.8E-05 1
rs199473320 0.882 0.120 3 38550878 missense variant G/C snv 6.0E-05 4.0E-04 1
rs193922726 1.000 0.080 3 38551188 missense variant G/A;C snv 6.0E-05 1
rs45627438 0.925 0.080 3 38604025 missense variant C/T snv 5.8E-05 2.8E-05 1
rs199473159 1.000 0.080 3 38587471 missense variant C/T snv 5.6E-05 2.1E-05 1
rs199473078 1.000 0.120 3 38609929 missense variant C/G snv 5.6E-05 4.2E-05 1
rs137854602 0.925 0.080 3 38555664 missense variant G/A snv 5.6E-05 1.4E-05 1
rs199473112 0.925 0.080 3 38605956 missense variant G/A;C snv 4.1E-06; 5.3E-05 1
rs199473048 1.000 0.120 3 38633166 missense variant C/T snv 5.3E-05 5.6E-05 1
rs199473192 1.000 0.120 3 38579425 missense variant G/A snv 4.9E-05 2.1E-04 1
rs199473047 1.000 0.120 3 38633180 missense variant C/G;T snv 4.8E-05 1
rs199473111 1.000 3 38606007 stop gained C/A;T snv 4.8E-05 6.3E-05 1
rs199473090 1.000 0.080 3 38608194 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 4.8E-05 1
rs199473050 1.000 0.080 3 38633098 missense variant A/C snv 4.4E-05 1.4E-05 1
rs199473640 1.000 0.120 3 38550338 missense variant G/A snv 4.3E-05 2.1E-05 1
rs199473220 0.882 0.120 3 38562422 missense variant C/A snv 4.2E-05 2.8E-05 1
rs45609733 0.925 0.120 3 38598998 missense variant G/A snv 4.0E-05 1.9E-04 2
rs199473634 0.925 0.120 3 38551036 missense variant G/A snv 4.0E-05 7.7E-05 2
rs199473283 1.000 0.120 3 38551495 missense variant C/A;G;T snv 4.0E-05 1
rs199473294 0.925 0.080 3 38551334 missense variant C/G;T snv 4.0E-06; 4.0E-05 1