Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13141641 1.000 0.040 4 144585304 intron variant T/C snv 0.32 8
rs35652124
NFE2L2
0.790 0.320 2 177265345 intron variant T/C snv 0.29 8
rs13118928 0.925 0.040 4 144565237 intron variant A/G snv 0.33 7
rs1927907
TLR4
0.790 0.320 9 117710486 intron variant C/T snv 0.18 7
rs2568494
IREB2
0.851 0.080 15 78448622 intron variant G/A snv 0.36 7
rs37973
GLCCI1 ; GLCCI1-DT
0.807 0.280 7 7968245 intron variant G/A;C snv 7
rs754388
RIN3
0.882 0.120 14 92649065 intron variant G/C;T snv 7
rs7655625 1.000 0.040 4 144564763 intron variant T/C;G snv 7
rs7671167
FAM13A
0.925 0.040 4 88962828 intron variant C/T snv 0.53 7
rs10922109
CFH
0.827 0.080 1 196735502 intron variant C/A snv 0.46 6
rs12504628
LOC105377462
1.000 0.040 4 144515172 intron variant T/C snv 0.33 6
rs1317286
CHRNA3
0.925 0.120 15 78603787 intron variant A/G snv 0.30 6
rs1529672
RARB
1.000 0.040 3 25479091 intron variant C/A;T snv 6
rs1840680
PTX3 ; VEPH1
0.807 0.200 3 157438240 intron variant A/G snv 0.59 6
rs4795405
LRRC3C
0.851 0.160 17 39932164 intron variant T/A;C snv 6
rs951266
CHRNA5
0.882 0.080 15 78586199 intron variant G/A snv 0.26 6
rs9788721
HYKK
1.000 0.040 15 78510527 intron variant C/T snv 0.65 6
rs138544659
CHRNA3
1.000 0.040 15 78608359 intron variant T/G snv 0.28 5
rs1512288 1.000 0.040 4 144570129 intron variant G/A snv 0.42 5
rs1828591
LOC105377462
1.000 0.040 4 144559628 intron variant A/G snv 0.43 5
rs190065944
CHRNA5
0.925 0.080 15 78567268 intron variant G/A snv 3.4E-03 5
rs2013701
FAM13A
1.000 0.040 4 88963935 intron variant G/T snv 0.51 5
rs2076295
DSP
0.882 0.080 6 7562999 intron variant T/G snv 0.46 5
rs2656069
IREB2
0.882 0.080 15 78453365 intron variant C/G;T snv 5
rs3753395
CFH
0.882 0.120 1 196717522 intron variant A/G;T snv 5