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
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 8
rs12429545 13 53528071 intron variant G/A;T snv 0.12 4
rs12731372 1 118310352 regulatory region variant C/T snv 0.19 3
rs1443512 12 53948900 downstream gene variant A/C;T snv 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
rs1884897 20 6632185 regulatory region variant A/G;T snv 5
rs1928295 9 117616205 intergenic variant T/C snv 0.45 3
rs4141278 7 25817905 intergenic variant T/C snv 0.16 3
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 8
rs6556301 5 177100576 downstream gene variant G/T snv 0.33 5
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 9
rs7164727 15 72801650 downstream gene variant C/G;T snv 3
rs7536458 1 118321979 intergenic variant T/G snv 0.23 5
rs8066985 17 70457204 intergenic variant A/G snv 0.56 4
rs979012 1.000 0.080 20 6642727 intergenic variant T/C snv 0.67 5
rs998584 6 43790159 downstream gene variant C/A snv 0.41 10
rs1879529
ACAN
15 88871064 intron variant G/T snv 0.28 3
rs2371767
ADAMTS9-AS2
3 64732582 intron variant G/C snv 0.38 5
rs7162542
ADAMTSL3
15 83845538 intron variant C/A;G;T snv 4