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
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 16
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 9
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 8
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 8
rs2571445
TNS1
0.925 0.080 2 217818431 missense variant A/G;T snv 0.62 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
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs13141641 1.000 0.040 4 144585304 intron variant T/C snv 0.32 6
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 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
rs2853677
TERT
0.724 0.240 5 1287079 3 prime UTR variant G/A snv 0.63 6
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 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
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