Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs712 0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs121913412 0.724 0.280 3 41224633 missense variant A/C;G;T snv 19
rs629849 0.827 0.160 6 160073377 missense variant A/C;G;T snv 0.90 0.91 9
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs3742330 0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02 24
rs750521832 0.732 0.200 11 102718452 missense variant A/G snv 4.0E-06 14
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 29
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs137854575
APC
0.807 0.120 5 112838399 stop gained C/A;G;T snv 4.7E-04 9
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs14035
RAN
0.742 0.320 12 130876696 3 prime UTR variant C/T snv 0.33 15
rs1801157 0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46