Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs763802417 0.882 0.040 X 100862805 missense variant G/A snv 5.9E-06 5
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs11053646 0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs696217 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs10903323 0.807 0.160 8 10292057 intron variant A/G snv 0.15 8
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs12740374 0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 16
rs752596535 0.752 0.200 19 11105407 stop gained C/A;G;T snv 1.6E-05 14
rs688 0.742 0.400 19 11116926 synonymous variant C/T snv 0.39 0.34 16
rs544456198 0.790 0.120 19 11116930 missense variant G/T snv 8.0E-06 2.8E-05 9
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs11066001 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 15
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs201058276
F7
0.776 0.240 13 113118731 missense variant G/A;C snv 4.8E-05; 4.0E-06 11
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs3135506 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
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
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174