Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042838
PGR
0.742 0.240 11 101062681 missense variant C/A;G snv 0.13; 4.0E-06 12
rs10895068 0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02 14
rs743572 0.672 0.360 10 102837395 5 prime UTR variant A/G;T snv 0.40; 8.1E-06 24
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs1805097 0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 22
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs3783553 0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1219648 0.716 0.320 10 121586676 intron variant A/G;T snv 17
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs34330 0.724 0.280 12 12717761 5 prime UTR variant T/C snv 0.70 15
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs2308321 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 29
rs112843513 0.851 0.120 3 133600730 3 prime UTR variant G/- del 4
rs115160714 0.807 0.200 3 133601021 3 prime UTR variant G/A snv 5.8E-03 9
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77