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
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs6280 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs397514698 0.667 0.400 9 77797577 missense variant C/T snv 52
rs1143634 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47