Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs55819519 0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04 40
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 37
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs2227983 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 31
rs17235409 0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs3761549 0.724 0.480 X 49260888 intron variant G/A snv 9.6E-02 18
rs2302254 0.752 0.240 17 51153539 5 prime UTR variant C/T snv 0.22 15
rs1927914 0.732 0.520 9 117702447 upstream gene variant G/A snv 0.52 14
rs670 0.763 0.360 11 116837697 5 prime UTR variant C/T snv 0.17 13
rs16949649 0.776 0.200 17 51152947 upstream gene variant T/C snv 0.39 12
rs1057519855 0.776 0.120 11 533873 missense variant CT/AC;TC mnv 11
rs1204382931 0.790 0.160 2 38075270 missense variant A/C snv 4.3E-06 10
rs391957 0.763 0.240 9 125241745 non coding transcript exon variant T/C snv 0.72 10
rs1056892 0.882 0.160 21 36146408 missense variant G/A snv 0.37 0.39 6
rs3917412 1.000 0.040 1 169731361 intron variant T/A;C;G snv 4
rs746830376 0.925 0.200 1 22784501 missense variant G/A snv 2.4E-05 3.5E-05 4
rs747489687 0.925 0.080 8 6444626 frameshift variant AAGAAATATTGCA/- delins 2.3E-04 1.0E-04 4
rs2830581 1.000 0.080 21 26921481 3 prime UTR variant G/A;C snv 3
rs894151 1.000 0.080 8 95226180 intron variant T/C snv 0.39 2