Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs2569190
CD14 ; TMCO6
0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs153109
IL27
0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs2071286
NOTCH4
0.752 0.280 6 32212119 intron variant C/T snv 0.17 12
rs4969170
LOC101928674
0.752 0.440 17 78364457 intron variant A/C;G snv 0.54 11
rs10877012
CYP27B1 ; METTL1
0.763 0.280 12 57768302 intron variant G/C;T snv 10
rs4374383
MERTK
0.776 0.200 2 112013193 intron variant A/G snv 0.58 10
rs7270101
ITPA
0.776 0.200 20 3213247 intron variant A/C snv 8.7E-02 9.7E-02 10
rs1993116
CYP2R1
0.827 0.200 11 14888688 intron variant A/G snv 0.65 8
rs7944926
NADSYN1
0.807 0.200 11 71454579 intron variant A/G snv 0.54 7
rs1012068
DEPDC5
0.827 0.160 22 31869917 intron variant T/G snv 0.37 5
rs16851720
RNF7
0.827 0.120 3 141744456 intron variant A/C snv 0.21 5
rs17047200
TLL1
0.827 0.200 4 166008836 intron variant A/T snv 0.18 5
rs5998152
DEPDC5
0.827 0.160 22 31867176 intron variant T/C snv 0.37 5
rs11506105
EGFR
0.851 0.160 7 55152484 intron variant A/G snv 0.59 4
rs2267716
CRHR2
0.851 0.120 7 30677027 intron variant T/A;C snv 4
rs9695310
DDX58
0.851 0.120 9 32464137 intron variant G/C snv 0.52 4
rs6051702
C20orf194
0.882 0.120 20 3271278 intron variant A/C snv 0.19 3
rs12989760
SH3YL1
0.925 0.120 2 250470 intron variant T/C snv 2
rs10789491
EFCAB14
1.000 0.080 1 46713638 intron variant A/G snv 0.80 1
rs11697186
DDRGK1
1.000 0.080 20 3204477 intron variant A/C;T snv 7.0E-02 1
rs11966728 1.000 0.080 6 131955465 intron variant T/C snv 0.26 1