Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs199473141 1.000 0.120 3 38598923 missense variant A/G snv 1
rs199473099 1.000 0.120 3 38606700 missense variant G/A snv 1
rs199473135 1.000 0.120 3 38599031 missense variant G/A snv 1
rs199473283 1.000 0.120 3 38551495 missense variant C/A;G;T snv 4.0E-05 1
rs199473047 1.000 0.120 3 38633180 missense variant C/G;T snv 4.8E-05 1
rs199473192 1.000 0.120 3 38579425 missense variant G/A snv 4.9E-05 2.1E-04 1
rs199473138 1.000 0.120 3 38598981 stop gained C/A;G;T snv 4.0E-06; 2.8E-05 1
rs199473276 1.000 0.120 3 38554313 missense variant G/C snv 4.0E-06 1
rs199473128 1.000 0.120 3 38603867 stop gained C/A;T snv 8.0E-05 4.9E-05 1
rs199473218 1.000 0.120 3 38562495 stop gained C/A;T snv 4.0E-06 1
rs199473288 1.000 0.120 3 38551438 missense variant G/A;T snv 2.4E-05 1
rs199473195 1.000 0.120 3 38579384 missense variant C/T snv 1.3E-05 4.9E-05 1
rs199473110 1.000 0.120 3 38606052 missense variant C/A;T snv 1.6E-05 1
rs199473162 1.000 0.120 3 38586031 missense variant A/T snv 1
rs199473590 1.000 0.120 3 38581281 missense variant G/T snv 7.0E-06 1
rs199473048 1.000 0.120 3 38633166 missense variant C/T snv 5.3E-05 5.6E-05 1
rs199473150 1.000 0.120 3 38597799 missense variant G/A snv 1
rs199473257 1.000 0.120 3 38555756 missense variant C/T snv 1
rs199473224 0.925 0.120 3 38560404 missense variant C/G;T snv 1
rs199473632 1.000 0.120 3 38551072 missense variant T/C snv 1
rs199473126 1.000 0.120 3 38603890 missense variant C/A snv 3.2E-05 3.5E-05 1
rs199473311 0.882 0.120 3 38551070 missense variant T/C snv 7.0E-06 1
rs199473330 1.000 0.120 3 38550527 missense variant C/A;T snv 2.8E-05 1
rs199473334 1.000 0.120 3 38550443 missense variant A/T snv 1
rs199473314 1.000 0.120 3 38551043 missense variant C/T snv 1.6E-05 2.1E-05 1