Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs1927911 0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs281865545 0.695 0.360 17 64377836 missense variant C/G;T snv 18
rs765798193 0.732 0.320 12 121915884 frameshift variant G/-;GG delins 18
rs767649 0.695 0.480 21 25572410 intron variant T/A snv 7.5E-02 18
rs10434 0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 17
rs659366 0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 17
rs1617640
EPO
0.742 0.520 7 100719675 upstream gene variant C/A;G;T snv 15
rs1043307 0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs11200638 0.724 0.280 10 122461028 non coding transcript exon variant G/A snv 0.23 14