Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 17
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 8
rs56113850
CYP2A6
0.807 0.080 19 40847202 intron variant T/C snv 0.52 8
rs10737680
CFH
0.827 0.080 1 196710325 intron variant A/C snv 0.44 7
rs55781567
CHRNA5
0.851 0.080 15 78565644 5 prime UTR variant C/G snv 0.31 7
rs112635299
SERPINA2
1.000 0.040 14 94371805 downstream gene variant G/T snv 1.3E-02 7
rs13141641 1.000 0.040 4 144585304 intron variant T/C snv 0.32 6
rs10922109
CFH
0.827 0.080 1 196735502 intron variant C/A snv 0.46 6
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 6
rs9788721
HYKK
1.000 0.040 15 78510527 intron variant C/T snv 0.65 6
rs2869966
LOC105377327 ; FAM13A
1.000 0.040 4 88947927 intron variant C/T snv 0.47 6
rs2036527 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 5
rs7655625 1.000 0.040 4 144564763 intron variant T/C;G snv 5
rs1410996
CFH
0.807 0.240 1 196727803 intron variant G/A snv 0.46 5
rs138544659
CHRNA3
1.000 0.040 15 78608359 intron variant T/G snv 0.28 5
rs8040868
CHRNA3
0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 5
rs8042374
CHRNA3
0.807 0.200 15 78615690 intron variant A/G snv 0.29 5
rs190065944
CHRNA5
0.925 0.080 15 78567268 intron variant G/A snv 3.4E-03 5
rs55958997
CHRNB4
1.000 0.040 15 78623530 upstream gene variant C/A snv 0.32 5
rs2869967
FAM13A ; LOC105377327
0.827 0.120 4 88948181 intron variant T/C snv 0.49 5
rs11624512
RIN3
14 92644775 non coding transcript exon variant C/T snv 0.15 5
rs754388
RIN3
0.882 0.120 14 92649065 intron variant G/C;T snv 5
rs2316205 19 40840863 non coding transcript exon variant T/C snv 0.40 4
rs2274700
CFH
0.776 0.240 1 196713817 synonymous variant G/A;C;T snv 0.44 4
rs4243084
CHRNA3
1.000 0.040 15 78619330 intron variant G/C snv 0.30 4