Disease: Smoking Behaviors
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs998584 6 43790159 downstream gene variant C/A snv 0.41 10
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 9
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 8
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 6
rs1358980
LOC105375070
6 43796814 intergenic variant C/T snv 0.40 6
rs1812175
HHIP-AS1 ; HHIP
4 144653692 intron variant A/G snv 0.79 5
rs1884897 20 6632185 regulatory region variant A/G;T snv 5
rs2371767
ADAMTS9-AS2
3 64732582 intron variant G/C snv 0.38 5
rs3786897
PEPD
1.000 0.080 19 33402102 intron variant A/G snv 0.45 5
rs395962
LIN28B
6 104949543 intron variant T/G snv 0.72 5
rs6556301 5 177100576 downstream gene variant G/T snv 0.33 5
rs7536458 1 118321979 intergenic variant T/G snv 0.23 5
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
rs1443512 12 53948900 downstream gene variant A/C;T snv 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
rs4886782
LOXL1
1.000 0.040 15 73936469 intron variant G/A snv 0.27 4