Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs781703310 1.000 0.160 7 20742967 missense variant A/C;G snv 4.0E-06; 4.0E-06 1
rs1064793877 1.000 0.160 X 153743250 missense variant C/T snv 1
rs11146842 1.000 0.160 X 153743056 missense variant G/A snv 1
rs1170974058 1.000 0.160 X 153743495 stop gained C/A;T snv 2.8E-05 1
rs128624214 1.000 0.160 X 153737214 missense variant C/G snv 1
rs128624215 1.000 0.160 X 153736195 missense variant C/G;T snv 1
rs128624219 1.000 0.160 X 153736232 missense variant G/A snv 1
rs128624220 1.000 0.160 X 153736372 missense variant C/T snv 1
rs128624221 1.000 0.160 X 153736510 stop gained C/T snv 1
rs128624222 1.000 0.160 X 153737192 stop gained G/A;T snv 2.2E-05 1
rs128624224 1.000 0.160 X 153740155 missense variant C/G;T snv 1
rs150346282 1.000 0.160 X 153743031 missense variant G/A snv 1
rs1557054210 1.000 0.160 X 153736390 stop gained C/T snv 1
rs1557054745 1.000 0.160 X 153740135 missense variant G/A snv 1
rs1557054776 1.000 0.160 X 153740231 missense variant C/T snv 1
rs1557054873 1.000 0.160 X 153740711 missense variant G/A snv 1
rs1557054875 1.000 0.160 X 153740721 splice donor variant T/G snv 1
rs1557055253 1.000 0.160 X 153743024 frameshift variant GTGG/- delins 1
rs1557055260 1.000 0.160 X 153743032 missense variant A/G snv 1
rs1557055316 1.000 0.160 X 153743231 missense variant G/A snv 1
rs1557055337 1.000 0.160 X 153743328 missense variant C/T snv 1
rs1557055340 1.000 0.160 X 153743334 missense variant G/A;T snv 1
rs1557055392 1.000 0.160 X 153743494 frameshift variant -/GC delins 1
rs1557055398 1.000 0.160 X 153743500 missense variant C/T snv 1
rs1569541000 1.000 0.160 X 153736126 stop gained A/T snv 1