Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7969931 0.851 0.080 12 25089661 missense variant C/A;G snv 1.6E-05; 0.75 5
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs7813 0.689 0.360 17 744946 missense variant G/A;C snv 0.63 22
rs4072037 0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 22
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs2072454 0.763 0.160 7 55146655 synonymous variant C/T snv 0.51 0.51 9
rs6505162 0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs595961 0.807 0.160 1 35902179 intron variant A/G snv 0.30 0.37 6
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs16969968 0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs735482 0.742 0.160 19 45408744 missense variant A/C snv 0.21 0.20 16
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs2073498 0.763 0.280 3 50332115 missense variant C/A snv 9.6E-02 8.0E-02 12
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs63750447 0.716 0.200 3 37025749 missense variant T/A snv 2.7E-03 7.5E-04 17
rs372043866 0.732 0.240 17 39727965 missense variant G/A;C;T snv 3.2E-05; 2.4E-05; 1.2E-05 18
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70