Source: ALL
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
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs770374710 0.611 0.560 15 23645747 frameshift variant G/-;GG delins 87
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs587777893 0.658 0.240 1 11128107 missense variant G/A;T snv 67
rs61753219 0.672 0.400 6 42978330 missense variant G/A snv 3.6E-05 2.8E-05 64
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1276519904 0.645 0.520 1 226071445 missense variant A/G snv 63
rs1010184002 0.689 0.400 6 42978878 stop gained C/T snv 7.0E-06 60
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs886040971 0.683 0.280 8 115604339 stop gained G/A;T snv 56
rs796052243 0.695 0.520 4 122934574 inframe deletion CAA/- delins 54
rs1085307993 0.716 0.440 5 161331056 missense variant C/T snv 53
rs1553621496 0.677 0.440 2 209976305 splice donor variant T/G snv 53
rs4647924 0.600 0.520 4 1801844 missense variant C/A;G;T snv 4.2E-06; 4.2E-06 49
rs200661329 0.708 0.440 16 576255 splice donor variant G/A;C snv 5.7E-05 48
rs752298579 0.701 0.480 22 20061538 missense variant G/A snv 1.4E-04 7.0E-06 48