Disease: Smoking Behaviors
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 18
rs8040868
CHRNA3
0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 17
rs667282
CHRNA5
0.790 0.120 15 78571130 intron variant T/C snv 0.28 13
rs2036527 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 12
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 11
rs56113850
CYP2A6
0.807 0.080 19 40847202 intron variant T/C snv 0.52 10
rs6495309
CHRNB4 ; CHRNA3
0.807 0.080 15 78622903 upstream gene variant C/A;T snv 10
rs8042374
CHRNA3
0.807 0.200 15 78615690 intron variant A/G snv 0.29 10
rs17486278
CHRNA5
0.827 0.120 15 78575140 intron variant A/C snv 0.32 9
rs10519203
HYKK
0.851 0.080 15 78521704 intron variant G/A snv 0.67 8
rs1062980
IREB2
0.827 0.080 15 78500185 3 prime UTR variant T/C snv 0.39 8
rs12910984
CHRNA3
0.827 0.080 15 78599285 intron variant G/A;C;T snv 8
rs13141641 1.000 0.040 4 144585304 intron variant T/C snv 0.32 8
rs2036534
HYKK
0.827 0.080 15 78534606 3 prime UTR variant T/C snv 0.26 8
rs6495308
CHRNA3
0.851 0.160 15 78615314 intron variant T/C snv 0.29 8
rs13180
IREB2
0.851 0.160 15 78497146 synonymous variant C/T snv 0.54 0.51 7
rs2568494
IREB2
0.851 0.080 15 78448622 intron variant G/A snv 0.36 7
rs931794
HYKK
0.851 0.080 15 78533838 3 prime UTR variant G/A;C snv 7
rs938682
CHRNA3
0.851 0.080 15 78604205 intron variant G/A snv 0.72 7
rs11637630
CHRNA3
0.882 0.080 15 78607377 intron variant G/A snv 0.71 6
rs1317286
CHRNA3
0.925 0.120 15 78603787 intron variant A/G snv 0.30 6