Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs374512193 0.925 0.120 8 42838177 missense variant T/C snv 5.2E-05 5.6E-05 4
rs1064797344 1.000 0.080 8 42843033 missense variant G/A snv 1
rs1131691345 1.000 0.080 8 42838099 stop gained G/A;C snv 1
rs118204013 1.000 0.080 8 42839212 missense variant A/G snv 1
rs138918468 1.000 0.080 8 42838108 missense variant C/T snv 2.4E-05 2.8E-05 1
rs1554599616 1.000 0.080 8 42838315 stop gained G/A snv 1
rs1554599712 1.000 0.080 8 42839322 frameshift variant T/- delins 1
rs1554599983 1.000 0.080 8 42843088 stop gained G/A snv 1
rs1563644456 1.000 0.080 8 42838298 frameshift variant -/G delins 1
rs1563644810 1.000 0.080 8 42839244 inframe deletion TTG/- delins 1
rs1563646198 1.000 0.080 8 42843093 start lost A/G snv 1
rs267607111 1.000 0.080 8 42839187 missense variant T/C snv 7.0E-06 1
rs267607112 1.000 0.080 8 42843070 missense variant C/A snv 1
rs372080941 1.000 0.080 8 42839215 missense variant T/A;C snv 2.8E-05 1
rs377725442 1.000 0.080 8 42838030 missense variant C/T snv 4.0E-06 3.5E-05 1
rs387907176 1.000 0.080 8 42843025 missense variant T/C snv 1
rs387907177 1.000 0.080 8 42843027 missense variant T/G snv 1
rs759392096 1.000 0.080 8 42838083 missense variant T/C snv 8.0E-06 1
rs766483829 1.000 0.080 8 42843045 missense variant T/C snv 2.8E-05 1
rs767519301 1.000 0.080 8 42838098 missense variant C/T snv 1.2E-05 1
rs767952378 1.000 0.080 8 42839367 missense variant C/T snv 4.0E-06 1
rs768017019 1.000 0.080 8 42839206 missense variant A/G snv 4.0E-06 7.0E-06 1
rs769988455 1.000 0.080 8 42838197 missense variant T/C snv 1.6E-05 1.4E-05 1
rs950435041 1.000 0.080 8 42838209 missense variant A/G snv 1.6E-05 2.1E-05 1