Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1168278189 1.000 0.120 16 88837740 missense variant G/A snv 4.0E-06 1
rs118204435 1.000 0.120 16 88836222 missense variant G/C snv 1
rs118204436 1.000 0.120 16 88841001 missense variant A/G snv 1
rs118204439 1.000 0.120 16 88818072 stop gained G/A;C snv 5.2E-06 1
rs118204440 1.000 0.120 16 88818029 missense variant T/C snv 1
rs118204441 1.000 0.120 16 88841936 missense variant G/A;C snv 1
rs118204445 1.000 0.120 16 88842745 missense variant A/C snv 1
rs118204448 1.000 0.120 16 88835240 missense variant C/A;T snv 1
rs118204449 1.000 0.120 16 88835794 stop gained C/T snv 1
rs1204485789 1.000 0.120 16 88818039 missense variant G/A snv 1
rs1209154325 1.000 0.120 16 88842711 missense variant G/A snv 4.0E-06 1
rs1263679818 1.000 0.120 16 88842714 missense variant C/T snv 4.0E-06 1
rs1269110043 1.000 0.120 16 88832025 missense variant C/G snv 8.0E-06 1
rs1288687291 1.000 0.120 16 88843167 synonymous variant T/C snv 7.4E-06 1
rs1296755011 1.000 0.120 16 88842799 missense variant C/T snv 4.0E-06 1
rs1301146300 1.000 0.120 16 88837721 missense variant A/C snv 4.0E-06 1
rs1301198698 1.000 0.120 16 88837690 missense variant G/C snv 1
rs1308500116 1.000 0.120 16 88837722 missense variant A/G snv 1.2E-05 1
rs1401175486 1.000 0.120 16 88818009 missense variant T/A;C snv 1
rs141340188 1.000 0.120 16 88841965 missense variant G/A;T snv 8.2E-06 1
rs1421990673 1.000 0.120 16 88842792 missense variant G/A snv 4.0E-06 1
rs1567526805 1.000 0.120 16 88832000 stop gained G/A snv 1
rs1567538216 1.000 0.120 16 88842831 splice acceptor variant T/C snv 1
rs191519947 1.000 0.120 16 88842807 missense variant A/C;G snv 4.8E-05; 3.3E-04 1
rs200763834 1.000 0.120 16 88824869 missense variant C/G snv 1