Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 73
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs727503094 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 41
rs12203592 0.649 0.320 6 396321 intron variant C/T snv 0.10 38
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 37
rs78378222 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs1444669684 0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs1057519695 0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 33