Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs199473300 1.000 0.120 3 38551204 missense variant G/T snv 1.4E-05 1
rs199473259 1.000 0.120 3 38555735 missense variant G/C snv 1
rs199473256 1.000 0.120 3 38556460 missense variant A/C;G snv 1
rs199473321 0.925 0.120 3 38550856 missense variant T/C snv 1
rs199473108 0.925 0.120 3 38606071 missense variant G/A;C;T snv 1.2E-05 1
rs137854610 0.925 0.120 3 38550895 missense variant C/T snv 2.8E-05 1.7E-04 1
rs199473325 1.000 0.120 3 38550671 stop gained C/A;G;T snv 3.2E-05; 2.0E-05 1
rs199473109 1.000 0.120 3 38606064 missense variant G/C snv 1
rs199473553 1.000 0.120 3 38633154 missense variant G/A snv 8.1E-06 1.4E-05 1
rs28937316 0.882 0.120 3 38551441 missense variant C/A;T snv 4.0E-06 1
rs199473598 1.000 0.120 3 38566558 stop gained C/A;T snv 1.2E-05 1
rs199473572 1.000 0.120 3 38604863 stop gained C/A;T snv 2.8E-05 1.2E-04 1
rs199473264 1.000 0.120 3 38555706 missense variant T/C snv 1
rs199473136 1.000 0.120 3 38599026 missense variant C/G;T snv 4.1E-06; 1.2E-05 1
rs199473094 1.000 0.120 3 38606791 missense variant G/A snv 4.0E-06 7.0E-06 1
rs199473202 1.000 0.120 3 38575367 missense variant T/G snv 1
rs199473227 1.000 0.120 3 38560380 missense variant G/C snv 4.0E-06 1
rs137854614 0.882 0.120 3 38550988 missense variant T/C snv 1
rs45465995 1.000 0.120 3 38550683 missense variant G/A snv 7.6E-05; 8.0E-06 9.1E-05 1
rs199473105 1.000 0.120 3 38606099 missense variant A/G snv 7.0E-06 1
rs61737825 1.000 0.120 3 38581248 missense variant G/A;C snv 4.1E-06 1
rs199473049 1.000 0.120 3 38633150 missense variant C/T snv 1.2E-05 2.1E-05 1
rs28937317 0.882 0.120 3 38560418 missense variant T/C snv 1
rs199473616 1.000 0.120 3 38555731 missense variant C/A snv 4.0E-06 1
rs199473043 1.000 0.120 3 38633282 missense variant C/A snv 1