Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1801157 0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs769985775
DMD
0.851 0.160 X 32448630 synonymous variant T/C snv 5.7E-06 9.5E-06 6
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs17883901 0.851 0.240 6 53545239 intron variant G/A;T snv 6.2E-02 6
rs696217 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs4746 0.708 0.400 6 38682852 missense variant T/A;G snv 0.36 21
rs2736654 0.882 0.120 6 38682852 missense variant T/A;G snv 4
rs713041 0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16
rs2518344 6 101327270 intron variant A/G snv 0.62 1
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs10499298 6 155812936 intergenic variant C/T snv 0.12 1
rs10499299 6 155812754 intergenic variant A/G snv 0.14 1
rs17827966 6 155817575 regulatory region variant T/C snv 0.12 1
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs7533564 0.925 0.120 1 78360228 intron variant C/T snv 0.92 4
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs713050 6 44124392 intron variant T/G snv 0.14 1
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
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33