Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs28362491
LOC105377621 ; NFKB1
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs2430561
IFNG ; IFNG-AS1
0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 43
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs5743836
TLR9
0.658 0.440 3 52226766 intron variant A/G snv 0.20 31
rs4246215
FADS2 ; FEN1
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 29
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs10754558
NLRP3
0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs35761398
CNR2
0.701 0.520 1 23875429 missense variant TT/CC mnv 19