Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs4977574 0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs1063192 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 24
rs4977756 0.683 0.440 9 22068653 intron variant G/A snv 0.64 24
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs3217992 0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 22
rs2227306 0.677 0.680 4 73741338 intron variant C/T snv 0.31 21