Disease: Smoking
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 6
rs10842707 12 26318431 intron variant C/G;T snv 4
rs10923712
TBX15
1 118962811 intron variant G/A snv 0.56 4
rs12317176
CCDC92 ; DNAH10
12 123920171 intron variant T/C snv 0.39 3
rs12429545 13 53528071 intron variant G/A;T snv 0.12 4
rs12493901
FNDC3B
3 172204265 intron variant G/A snv 0.37 3
rs12991495
DNMT3A
2 25263901 intron variant T/C snv 0.22 3
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
rs17024393
GNAT2
1 109612066 intron variant T/C snv 4.6E-02 4
rs1812175
HHIP-AS1 ; HHIP
4 144653692 intron variant A/G snv 0.79 5
rs1879529
ACAN
15 88871064 intron variant G/T snv 0.28 3
rs2294239
ZNRF3
22 29053489 intron variant A/G snv 0.36 4
rs2365389
FHIT
3 61250788 intron variant C/T snv 0.56 3
rs2371767
ADAMTS9-AS2
3 64732582 intron variant G/C snv 0.38 5
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 9
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
rs3817334
MTCH2
1.000 0.080 11 47629441 intron variant C/T snv 0.36 4
rs395962
LIN28B
6 104949543 intron variant T/G snv 0.72 5
rs4239436
CABLES1
18 23151966 intron variant A/G snv 0.81 3
rs4765219
CCDC92
12 123955563 intron variant C/A;T snv 3
rs4886782
LOXL1
1.000 0.040 15 73936469 intron variant G/A snv 0.27 4
rs6090583
EYA2
20 46930192 intron variant A/C;G snv 3
rs6437061
DIS3L2
2 232320342 intron variant A/C snv 0.56 3