Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1183194405
F2
0.716 0.440 11 46719773 missense variant G/A;T snv 4.5E-06; 4.5E-06 19
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121908686 0.882 0.120 22 38112558 missense variant C/T snv 9.0E-05 6
rs121918474 0.763 0.320 3 93905799 missense variant T/C snv 2.8E-05 1.4E-05 11
rs1255283120 0.807 0.160 1 11792345 missense variant G/A snv 4.0E-06 7.0E-06 7
rs1312546120
F5
0.807 0.160 1 169541191 missense variant T/C snv 4.0E-06 7
rs13306190 0.807 0.320 2 21032408 missense variant G/A;C;T snv 1.7E-04; 8.0E-06 7
rs1369837875 0.882 0.200 22 38128276 synonymous variant G/A snv 4
rs1371086615
APC
0.851 0.120 5 112828890 missense variant G/A snv 4.0E-06 7.0E-06 4
rs141012637 0.851 0.320 18 63901881 stop gained C/A;T snv 7.0E-05 4
rs1431515214
APC
0.925 0.080 5 112839790 missense variant G/A snv 4.0E-06 2
rs144246695 0.851 0.160 4 83310887 missense variant G/A snv 8.0E-06 4
rs1482856709 0.925 0.080 3 93900887 missense variant G/A snv 3
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs1799963
F2
0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 25
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs2066865
FGG
0.807 0.240 4 154604124 downstream gene variant G/A snv 0.26 10
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs368927897 0.790 0.240 9 5072541 missense variant G/A;T snv 2.8E-05; 6.4E-05 9
rs370975770 1.000 0.080 22 38115666 missense variant C/T snv 8.9E-06 2.8E-05 1
rs3789683
F3
0.925 0.200 1 94530506 missense variant C/T snv 6.5E-03 1.0E-02 3
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306