Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs8193037 0.752 0.320 6 52186311 upstream gene variant G/A;T snv 12
rs112443954 1.000 0.080 6 13574259 upstream gene variant G/C snv 0.27 1
rs2804924 1.000 0.080 6 13574110 upstream gene variant G/A;C;T snv 1
rs9978223 1.000 0.080 21 33398052 upstream gene variant G/A snv 0.24 1
rs200478651
F7
1.000 0.080 13 113118414 splice region variant C/A;T snv 8.4E-06; 2.1E-05 1
rs767910122 0.724 0.280 7 150948446 frameshift variant -/GTCCG ins 4.4E-05 17
rs794728448 0.724 0.280 7 150948445 frameshift variant CT/G delins 17
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs11571836 0.827 0.200 13 32399302 3 prime UTR variant A/G;T snv 6
rs225015 0.882 0.160 14 80201236 3 prime UTR variant G/A snv 0.37 5
rs1050286 0.882 0.160 12 10158964 3 prime UTR variant T/C snv 0.40 3
rs12095080 1.000 0.080 1 53911057 3 prime UTR variant A/G snv 0.12 2
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1799943 0.925 0.080 13 32316435 5 prime UTR variant G/A;C;T snv 0.25 5
rs1076991 0.925 0.200 14 64388323 5 prime UTR variant T/C;G snv 0.45; 8.1E-06 2
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs4244285 0.695 0.360 10 94781859 synonymous variant G/A;C snv 0.18 18
rs771676129 0.827 0.080 7 80671082 synonymous variant C/T snv 4.0E-06 7
rs999947969 0.827 0.080 7 80671145 synonymous variant C/T snv 7
rs1805120 0.882 0.080 7 150952443 synonymous variant G/A snv 0.30 0.26 3
rs1049194905 0.925 0.080 3 38604063 synonymous variant A/G snv 2
rs184934308 0.925 0.080 3 38575342 synonymous variant G/A snv 4.1E-04 9.1E-05 2
rs201698592 0.925 0.080 11 2847916 synonymous variant C/T snv 1.7E-04 2.8E-05 2
rs740952 0.925 0.080 7 150952515 synonymous variant G/A;T snv 0.30; 7.2E-05 2