Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs215607
PDE1C
7 32298725 missense variant G/A snv 0.79 0.77 1
rs4079366
CYP2A7
19 40878770 missense variant T/A;C snv 1.6E-05; 0.76 2
rs13180
IREB2
0.851 0.160 15 78497146 synonymous variant C/T snv 0.54 0.51 3
rs2276824
PBRM1
3 52603470 intron variant C/G snv 0.54 0.61 3
rs4542783
MYO1F
19 8577276 non coding transcript exon variant T/C snv 0.53 0.52 3
rs7917772
SFXN2
10 102727686 3 prime UTR variant G/A;C snv 0.46 3
rs8040868
CHRNA3
0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 5
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 5
rs2071449
HOXC4 ; HOXC5 ; MIR615
12 54034227 intron variant C/A;T snv 0.35; 4.2E-06 4
rs3825807
ADAMTS7
0.807 0.120 15 78796769 missense variant A/G snv 0.34 0.33 2
rs569207
CHRNA5
15 78580777 intron variant C/G;T snv 0.34 2
rs2274432
TSEN15
1 184051811 missense variant G/A snv 0.33 0.28 4
rs2277545
ADAMTS7
15 78791249 intron variant T/C snv 0.33 0.31 1
rs16957091
CDAN1
15 42725228 synonymous variant T/A;C;G snv 4.0E-06; 0.29 2
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 6
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 3
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs16906252
MGMT
0.732 0.200 10 129467281 synonymous variant C/T snv 5.5E-02 5.1E-02 2
rs61731371
SNX25
4 185351567 synonymous variant A/G snv 4.9E-02 3.7E-02 2
rs60866311
NPAS2 ; NPAS2-AS1
2 100975599 non coding transcript exon variant T/G snv 4.1E-02 7.2E-02 2
rs148215758
PHF8
X 54017674 synonymous variant A/C;T snv 2.6E-02 2
rs73085315
MUC4
3 195778256 intron variant G/C snv 2.5E-02 0.10 2
rs61880854
MMP26 ; OR52R1
11 4803398 intron variant G/A snv 2.4E-02 2.3E-02 2
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 17
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18