Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31 21
rs2227307
CXCL8
0.851 0.240 4 73740952 intron variant T/G snv 0.45 6
rs397508266
CFTR
0.851 0.160 7 117589467 intron variant A/G snv 2.8E-05 4
rs75039782
CFTR
0.851 0.160 7 117639961 intron variant C/G;T snv 4
rs7512462
SLC26A9
0.882 0.200 1 205930467 intron variant T/C snv 0.38 4
rs201716473
CFTR
0.925 0.160 7 117602800 intron variant A/G snv 4.0E-06; 1.6E-03 1.1E-03 2
rs73715573
CFTR-AS1 ; CFTR
0.925 0.160 7 117548630 intron variant T/G snv 8.6E-03; 5.9E-05 9.0E-03 2
rs76151804
CFTR
0.925 0.160 7 117611555 intron variant A/G snv 4.2E-05 6.3E-05 2
rs9268905
HLA-DRB9
0.925 0.280 6 32464300 intron variant G/C snv 0.29 2
rs117230773
HLA-DRB9
1.000 0.120 6 32465964 intron variant G/A snv 1
rs1554388867
CFTR
1.000 0.120 7 117589470 intron variant A/G snv 1
rs1554398510
CFTR
1.000 0.120 7 117675861 intron variant C/T snv 1
rs17140229
CFTR
1.000 0.120 7 117590229 intron variant T/C snv 9.9E-02 1
rs2688482
MUC4
1.000 0.120 3 195802247 intron variant T/C snv 0.66 1
rs3103933
MUC4
1.000 0.120 3 195758569 intron variant A/G;T snv 1
rs397508261
CFTR
1.000 0.120 7 117589476 intron variant G/A;T snv 1
rs56302516
SLC9A3
1.000 0.120 5 518319 intron variant C/G;T snv 1
rs9300298
ADIPOR2
1.000 0.120 12 1757038 intron variant T/A snv 0.55 1
rs12793173
LOC102723568
0.925 0.160 11 34812657 intergenic variant T/C snv 0.18 2
rs5952223 1.000 0.120 X 116255308 intergenic variant C/T snv 0.29 1
rs7879546 1.000 0.120 X 116217020 intergenic variant T/C snv 1
rs871799 1.000 0.120 1 203200743 intergenic variant C/G snv 0.18 1
rs7929679
LOC102723568
0.925 0.120 11 34784302 regulatory region variant A/G snv 0.54 2