Disease: Smoking
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7801581
HOXA11-AS ; HOXA11
7 27184152 intron variant C/T snv 0.24 5
rs979012 1.000 0.080 20 6642727 intergenic variant T/C snv 0.67 5
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
rs12429545 13 53528071 intron variant G/A;T snv 0.12 4
rs12885454
LOC102724934
14 29267632 non coding transcript exon variant C/A snv 0.27 4
rs1443512 12 53948900 downstream gene variant A/C;T snv 4
rs17024393
GNAT2
1 109612066 intron variant T/C snv 4.6E-02 4
rs17819328 3 12447843 intergenic variant T/A;G snv 4
rs2274432
TSEN15
1 184051811 missense variant G/A snv 0.33 0.28 4
rs2294239
ZNRF3
22 29053489 intron variant A/G snv 0.36 4
rs2645294
WARS2
1 119031964 3 prime UTR variant C/T snv 0.59 4
rs3817334
MTCH2
1.000 0.080 11 47629441 intron variant C/T snv 0.36 4
rs4886782
LOXL1
1.000 0.040 15 73936469 intron variant G/A snv 0.27 4
rs7162542
ADAMTSL3
15 83845538 intron variant C/A;G;T snv 4
rs8066985 17 70457204 intergenic variant A/G snv 0.56 4
rs9435732
MFAP2
1 16981663 intron variant C/G;T snv 4
rs12317176
CCDC92 ; DNAH10
12 123920171 intron variant T/C snv 0.39 3
rs12493901
FNDC3B
3 172204265 intron variant G/A snv 0.37 3
rs12731372 1 118310352 regulatory region variant C/T snv 0.19 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