Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1047840 0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs3783553 0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs5742909 0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 40
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs11134527 0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82