Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4957014 0.752 0.160 5 287899 intron variant T/G snv 0.74 11
rs12529 0.776 0.280 10 5094459 missense variant C/G snv 0.50 0.45 10
rs1130214 0.742 0.280 14 104793397 5 prime UTR variant C/A snv 0.31 12
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
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
rs4143815 0.689 0.400 9 5468257 3 prime UTR variant G/C snv 0.23 20
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs402710 0.716 0.320 5 1320607 non coding transcript exon variant C/T snv 0.33 0.38 18
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs776223836 0.763 0.280 19 45364045 missense variant G/A snv 11
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs768623239 0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63