Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34712979
NPNT
1.000 0.040 4 105897896 splice region variant G/A;T snv 0.17 5
rs55958997
CHRNB4
1.000 0.040 15 78623530 upstream gene variant C/A snv 0.32 5
rs754388
RIN3
0.882 0.120 14 92649065 intron variant G/C;T snv 5
rs7655625 1.000 0.040 4 144564763 intron variant T/C;G snv 5
rs8040868
CHRNA3
0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 5
rs10519203
HYKK
0.851 0.080 15 78521704 intron variant G/A snv 0.67 4
rs12504628
LOC105377462
1.000 0.040 4 144515172 intron variant T/C snv 0.33 4
rs1295685
TH2LCRR ; IL13
0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 4
rs1529672
RARB
1.000 0.040 3 25479091 intron variant C/A;T snv 4
rs17486278
CHRNA5
0.827 0.120 15 78575140 intron variant A/C snv 0.32 4
rs17580
SERPINA1
0.776 0.160 14 94380925 missense variant T/A snv 2.3E-02 2.9E-02 4
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 4
rs2076295
DSP
0.882 0.080 6 7562999 intron variant T/G snv 0.46 4
rs2274700
CFH
0.776 0.240 1 196713817 synonymous variant G/A;C;T snv 0.44 4
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 4
rs2955083
EEFSEC
1.000 0.040 3 128242335 intron variant T/A snv 0.89 4
rs4243084
CHRNA3
1.000 0.040 15 78619330 intron variant G/C snv 0.30 4
rs4416442
LOC105377327 ; FAM13A
0.925 0.080 4 88945562 intron variant T/C snv 0.45 4
rs55853698
CHRNA5
0.882 0.080 15 78565597 5 prime UTR variant T/G snv 0.25 4
rs71636784
ZDHHC18
1.000 0.040 1 26842709 intron variant T/G snv 0.12 4
rs7953249
HNF1A-AS1
0.882 0.160 12 120965921 splice region variant G/A snv 0.59 4
rs8031948
HYKK
1.000 0.040 15 78523715 intron variant G/T snv 0.27 4
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 4
rs8042849
HYKK
1.000 0.040 15 78525587 intron variant C/T snv 0.65 4
rs8756
HMGA2
0.882 0.200 12 65965972 3 prime UTR variant C/A snv 0.56 4