Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs45517305 0.851 0.240 16 2081646 stop gained C/A;T snv 4
rs376285784 1.000 0.120 16 2064342 missense variant G/A snv 1.2E-05 2.1E-05 2
rs45514100 0.925 0.160 16 2079093 stop gained C/G;T snv 4.0E-06 2
rs45517234 0.925 0.160 16 2074251 stop gained C/T snv 2
rs752603642 0.925 0.160 16 2072888 missense variant C/T snv 4.0E-06 2
rs1060500931 0.925 0.120 16 2064302 stop gained C/T snv 1
rs1114167462 1.000 0.120 16 2062533 stop gained C/T snv 1
rs1430119276 1.000 0.120 16 2079096 missense variant G/T snv 7.0E-06 1
rs1459518095 1.000 0.120 16 2084552 missense variant C/G;T snv 4.2E-06 1
rs28934872 0.851 0.200 16 2070571 missense variant G/A snv 1
rs397514914 1.000 0.120 16 2071534 missense variant C/T snv 1
rs397514916 0.925 0.120 16 2083754 missense variant C/G;T snv 1
rs397515225 1.000 0.120 16 2080366 missense variant G/A;C snv 4.0E-06 1
rs45438205 0.925 0.120 16 2080365 missense variant C/T snv 7.0E-06 1
rs45469298 0.851 0.200 16 2070570 missense variant C/G;T snv 1
rs45487497 0.925 0.120 16 2058779 missense variant G/A snv 1
rs45509500 1.000 0.120 16 2072923 synonymous variant C/G;T snv 4.0E-06; 5.6E-05 1
rs45517259 0.925 0.120 16 2076142 missense variant G/A snv 1
rs45517278 1.000 0.120 16 2079090 missense variant G/T snv 1
rs754504918 1.000 0.120 16 2071816 missense variant G/A snv 1
rs764288120 1.000 0.120 16 2061983 missense variant T/C snv 4.0E-06 1
rs993614997 1.000 0.120 16 2081714 missense variant C/T snv 2.1E-05 1
rs45507199 0.925 0.120 16 2088294 missense variant G/A;C;T snv 1
rs45517423 1.000 0.120 16 2088569 missense variant C/T snv 1.5E-03 1.5E-03 1