Disease: Smoking
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10919388 1 170403362 intergenic variant A/C snv 0.71 4
rs6437061
DIS3L2
2 232320342 intron variant A/C snv 0.56 3
rs6090583
EYA2
20 46930192 intron variant A/C;G snv 3
rs1443512 12 53948900 downstream gene variant A/C;T snv 4
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 8
rs13083798
PBRM1
3 52615732 intron variant A/G snv 0.51 3
rs13191362
PRKN
6 162612318 intron variant A/G snv 8.7E-02 3
rs1812175
HHIP-AS1 ; HHIP
4 144653692 intron variant A/G snv 0.79 5
rs2294239
ZNRF3
22 29053489 intron variant A/G snv 0.36 4
rs3786897
PEPD
1.000 0.080 19 33402102 intron variant A/G snv 0.45 5
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 8
rs4239436
CABLES1
18 23151966 intron variant A/G snv 0.81 3
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 8
rs6804842
RARB
3 25064946 intron variant A/G snv 0.53 3
rs7830933
LOC107986930
8 23745811 intron variant A/G snv 0.24 3
rs8066985 17 70457204 intergenic variant A/G snv 0.56 4
rs1884897 20 6632185 regulatory region variant A/G;T snv 5
rs10132280 14 25458973 intergenic variant C/A snv 0.37 6
rs10804591 3 129615390 intergenic variant C/A snv 0.63 4
rs12885454
LOC102724934
14 29267632 non coding transcript exon variant C/A snv 0.27 4
rs998584 6 43790159 downstream gene variant C/A snv 0.41 10
rs7162542
ADAMTSL3
15 83845538 intron variant C/A;G;T snv 4
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs4765219
CCDC92
12 123955563 intron variant C/A;T snv 3
rs10842707 12 26318431 intron variant C/G;T snv 4