Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs10719 0.677 0.680 5 31401340 3 prime UTR variant A/G;T snv 0.69 24
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs28936379 0.807 0.120 1 226888977 missense variant A/C;G;T snv 4.0E-06 10
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4717806 0.776 0.200 7 73702147 intron variant T/A;C snv 9
rs4746 0.708 0.400 6 38682852 missense variant T/A;G snv 0.36 21
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs4151667 0.790 0.320 6 31946247 missense variant T/A snv 3.9E-02 3.4E-02 9
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82