Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs28933979
TTR
0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04 70
rs4149056 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs1556425596 0.752 0.240 21 45989967 intron variant C/T snv 37
rs28937900 0.752 0.160 19 46756276 missense variant C/A;T snv 1.0E-03 37
rs543860009 0.742 0.320 2 178589003 stop gained G/A;T snv 33
rs878854378 0.742 0.320 2 178533657 inframe deletion GTT/- delins 33
rs74315401 0.683 0.320 20 4699525 missense variant C/T snv 32
rs121908188 0.742 0.360 1 25809753 missense variant G/A;C snv 1.8E-04 25
rs199564797 0.742 0.360 1 25809150 missense variant G/A snv 1.2E-05 1.4E-05 25
rs745886248 0.742 0.360 1 25811710 missense variant G/A;C;T snv 4.3E-06; 4.3E-06; 4.3E-06 25
rs121908557 0.752 0.280 17 63957514 missense variant C/T snv 8.2E-06 1.4E-05 23
rs781565158 0.851 0.120 12 21452130 missense variant A/G snv 4.7E-05 2.1E-05 22
rs80338800 0.827 0.120 15 42387803 frameshift variant A/- delins 21
rs1565930588 0.882 0.160 12 119193787 frameshift variant TACTCAACATTTGG/- del 19
rs781049584
APP
0.724 0.280 21 26021917 missense variant T/G snv 8.2E-06 7.0E-06 18
rs1555377415 0.827 0.200 14 77027274 stop gained G/C snv 18
rs1815739 0.763 0.240 11 66560624 stop gained C/T snv 0.37 17
rs912001256 0.851 0.240 17 63947062 stop gained G/A snv 17
rs121918075
TTR
0.752 0.280 18 31598632 missense variant A/G snv 15
rs1563221666 0.882 0.120 8 22162694 missense variant C/T snv 14
rs387906789
VCP
0.742 0.200 9 35065352 missense variant G/A;C snv 4.0E-06 14
rs80338962 0.742 0.240 17 63941508 missense variant T/C snv 13
rs104894201 0.763 0.280 11 111908934 missense variant T/C snv 12