Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs199473190 1.000 0.040 3 38579474 missense variant C/G;T snv 8.2E-06 1
rs199473627 1.000 0.040 3 38551258 missense variant A/G snv 1
rs727504495 1.000 0.080 3 38550998 missense variant C/A;T snv 4.0E-06; 2.0E-05 1
rs28937319 1.000 0.080 3 38562485 missense variant G/A snv 7.0E-06 1
rs199473260 0.925 0.120 3 38555720 missense variant T/C snv 1.6E-05 3.5E-05 1
rs199473107 1.000 0.120 3 38606078 missense variant A/T snv 1
rs199473618 1.000 0.120 3 38554498 missense variant C/A;T snv 2.4E-05; 2.8E-04 1
rs199473594 1.000 0.120 3 38576676 missense variant C/T snv 1
rs199473569 1.000 0.120 3 38606051 missense variant G/T snv 1
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