Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs2004640 0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs2104286 0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs5029939 0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs1143679 0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs10488631 0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 13
rs11889341 0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs2205960 0.763 0.400 1 173222336 intergenic variant G/A;T snv 9