Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs397514698
GNAQ
0.667 0.400 9 77797577 missense variant C/T snv 52
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs2569190
CD14 ; TMCO6
0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs1800925
IL13 ; TH2LCRR
0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv 21
rs4696480
TLR2
0.716 0.400 4 153685974 intron variant T/A snv 0.45 19
rs1064795104
EXOC6B
0.790 0.440 2 72498492 stop gained A/C snv 17
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 16
rs10993994
MSMB
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54 15
rs36051895 0.716 0.240 9 4981866 upstream gene variant G/T snv 0.25 15
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 14
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60 14
rs387906760
STAT1
0.790 0.200 2 190995184 missense variant C/T snv 13
rs1800875
CMA1
0.742 0.360 14 24510132 upstream gene variant C/T snv 0.41 12
rs324011
STAT6
0.742 0.360 12 57108399 intron variant C/T snv 0.32 12
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 12
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 12
rs1059513
NAB2 ; STAT6
0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 11
rs1555483699
GRIN2A
0.851 0.120 16 9768994 missense variant C/T snv 10
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 10
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10