Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs2241880 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 37
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs5743836 0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs879253942 0.677 0.400 17 7673826 missense variant A/G snv 28
rs876658657 0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs148704956 0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06 19
rs13281615 0.716 0.360 8 127343372 intron variant A/G snv 0.43 18
rs3850641 0.716 0.400 1 173206693 intron variant A/G snv 0.14 17
rs132770 0.752 0.320 22 41621260 5 prime UTR variant A/G snv 0.83 14
rs1284806277
MOK
0.827 0.200 14 102251978 missense variant A/G snv 1.4E-05 13
rs11214077 0.752 0.120 11 112087953 missense variant A/G snv 6.6E-03 6.7E-03 12
rs746284240 0.763 0.240 12 68809243 missense variant A/G snv 11
rs13428812 0.827 0.120 2 25269598 intron variant A/G snv 0.31 9
rs568887534 0.807 0.240 8 30183156 missense variant A/G snv 4.0E-06 9
rs3819102 0.827 0.120 18 675307 intron variant A/G snv 4.5E-02 3.6E-02 8
rs762292600 0.925 0.080 6 151944316 missense variant A/G snv 4.0E-06 1.4E-05 7