Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs137854600 0.807 0.120 3 38551504 missense variant C/A;T snv 6
rs199473225 0.851 0.120 3 38560397 missense variant G/A;C snv 6
rs137854606 0.882 0.120 3 38604062 missense variant C/A snv 4
rs137854612 0.851 0.120 3 38560170 missense variant C/T snv 4
rs137854615 0.851 0.120 3 38550989 missense variant A/G snv 4
rs199473229 0.882 0.120 3 38560361 missense variant A/G snv 4
rs199473244 0.851 0.120 3 38557251 missense variant C/A snv 4
rs199473556 0.851 0.120 3 38630342 missense variant G/A snv 4
rs199473092 0.925 0.080 3 38608175 missense variant A/C snv 3
rs199473096 0.882 0.120 3 38606751 missense variant G/A snv 3
rs199473103 0.925 0.120 3 38606102 missense variant A/G snv 3
rs199473143 0.925 0.080 3 38597949 missense variant T/G snv 3
rs199473207 0.882 0.120 3 38566555 missense variant G/A snv 3
rs199473051 0.925 0.120 3 38633058 missense variant C/T snv 2
rs199473070 0.925 0.120 3 38613811 missense variant A/G;T snv 2
rs199473079 1.000 0.080 3 38609860 missense variant G/T snv 2
rs199473093 0.925 0.080 3 38606802 missense variant G/A snv 2
rs199473168 0.925 0.080 3 38585846 missense variant G/A snv 2
rs199473169 0.925 0.080 3 38585821 missense variant T/G snv 2
rs199473240 0.925 0.080 3 38560176 missense variant C/T snv 2
rs199473245 0.925 0.080 3 38557236 missense variant T/C snv 2
rs199473248 0.925 0.080 3 38556565 missense variant G/A snv 2
rs199473292 0.925 0.080 3 38551391 missense variant C/G;T snv 2
rs199473305 0.925 0.080 3 38551145 missense variant C/T snv 1.4E-05 2
rs199473322 0.925 0.080 3 38550823 missense variant C/G snv 2