Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs735482 0.742 0.160 19 45408744 missense variant A/C snv 0.21 0.20 16
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs1057519847 0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848 0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs121434568 0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs28929495 0.807 0.120 7 55174014 missense variant G/A;C;T snv 9
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11549467 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs10491121 0.882 0.120 17 36102943 upstream gene variant G/A snv 0.32 5
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs1057519824
MET
0.807 0.120 7 116783374 missense variant T/G snv 10
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306