Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs2571445 0.925 0.080 2 217818431 missense variant A/G;T snv 0.62 10
rs3811381
CR1
0.763 0.240 1 207616743 missense variant C/A;G snv 8.0E-06; 0.24 11
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs5370 0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs56149945 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs679620 0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs3025058 0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26