Disease: Smoking
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs395962
LIN28B
6 104949543 intron variant T/G snv 0.72 5
rs17024393
GNAT2
1 109612066 intron variant T/C snv 4.6E-02 4
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs1928295 9 117616205 intergenic variant T/C snv 0.45 3
rs12731372 1 118310352 regulatory region variant C/T snv 0.19 3
rs7536458 1 118321979 intergenic variant T/G snv 0.23 5
rs10923712
TBX15
1 118962811 intron variant G/A snv 0.56 4
rs2645294
WARS2
1 119031964 3 prime UTR variant C/T snv 0.59 4
rs12317176
CCDC92 ; DNAH10
12 123920171 intron variant T/C snv 0.39 3
rs4765219
CCDC92
12 123955563 intron variant C/A;T snv 3
rs17819328 3 12447843 intergenic variant T/A;G snv 4
rs7766106
RSPO3
6 127133993 intron variant C/T snv 0.44 3
rs10804591 3 129615390 intergenic variant C/A snv 0.63 4
rs6772896
CEP63 ; ANAPC13
3 134484505 intron variant C/T snv 0.68 3
rs1812175
HHIP-AS1 ; HHIP
4 144653692 intron variant A/G snv 0.79 5
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs13191362
PRKN
6 162612318 intron variant A/G snv 8.7E-02 3
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 6
rs9435732
MFAP2
1 16981663 intron variant C/G;T snv 4
rs10919388 1 170403362 intergenic variant A/C snv 0.71 4
rs12493901
FNDC3B
3 172204265 intron variant G/A snv 0.37 3
rs6556301 5 177100576 downstream gene variant G/T snv 0.33 5
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 8
rs2274432
TSEN15
1 184051811 missense variant G/A snv 0.33 0.28 4