Disease: Smoking
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10132280 14 25458973 intergenic variant C/A snv 0.37 6
rs10804591 3 129615390 intergenic variant C/A snv 0.63 4
rs10842707 12 26318431 intron variant C/G;T snv 4
rs10919388 1 170403362 intergenic variant A/C snv 0.71 4
rs10923712
TBX15
1 118962811 intron variant G/A snv 0.56 4
rs1167827
HIP1
7 75533848 3 prime UTR variant G/A snv 0.37 5
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
rs12731372 1 118310352 regulatory region variant C/T snv 0.19 3
rs12885454
LOC102724934
14 29267632 non coding transcript exon variant C/A snv 0.27 4
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
rs1358980
LOC105375070
6 43796814 intergenic variant C/T snv 0.40 6
rs1443512 12 53948900 downstream gene variant A/C;T snv 4
rs17024393
GNAT2
1 109612066 intron variant T/C snv 4.6E-02 4
rs17405819 8 75894349 intergenic variant T/C snv 0.24 3
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs17819328 3 12447843 intergenic variant T/A;G snv 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
rs1884897 20 6632185 regulatory region variant A/G;T snv 5
rs1928295 9 117616205 intergenic variant T/C snv 0.45 3
rs2245368
DTX2P1-UPK3BP1-PMS2P11 ; LOC105375361
7 76978826 non coding transcript exon variant C/T snv 0.80 3