Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10865710 0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs174537 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 23
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2266788 0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 19
rs281865545 0.695 0.360 17 64377836 missense variant C/G;T snv 18
rs3834458 0.807 0.200 11 61827449 intron variant T/- del 0.28 7
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs46522 0.807 0.120 17 48911235 non coding transcript exon variant C/T snv 0.40 8
rs4773144 0.827 0.080 13 110308365 intron variant A/G snv 0.42 7
rs4845625 0.851 0.080 1 154449591 intron variant T/C snv 0.60 9
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs7901695 0.851 0.160 10 112994329 intron variant T/C snv 0.34 6
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs911119 0.807 0.120 20 23632100 non coding transcript exon variant C/G;T snv 9
rs9319428 0.925 0.080 13 28399484 intron variant G/A snv 0.30 4
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262