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
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs1801320 0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12 15
rs1801321 0.790 0.160 15 40695367 5 prime UTR variant G/C;T snv 0.35 8
rs1899663 0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs4645978 0.827 0.120 1 15525539 intron variant C/A;T snv 8
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs11549467 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42