Disease: Smoking
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10031466
TRIML2
4 188094248 intron variant G/A snv 0.56 2
rs1003858
PAPPA
9 116202676 intron variant G/C snv 1.1E-02 2
rs10041657
FER
5 108816727 intron variant G/A snv 0.23 2
rs1014667
NRXN1
2 50521617 intron variant G/A;C snv 2
rs10269774
CDK6
7 92624658 intron variant G/A snv 0.36 2
rs10425738
CYP2G1P
19 40911822 non coding transcript exon variant G/A snv 0.74 2
rs10440708 5 173223484 downstream gene variant A/G snv 4.3E-02 2
rs10488693
DAGLA
11 61717684 intron variant C/T snv 6.0E-02 2
rs1049281
HLA-C
1.000 0.120 6 31268790 3 prime UTR variant T/C snv 0.68 2
rs10501157
TRAF6
11 36485319 3 prime UTR variant T/C snv 1.6E-02 2
rs10503023 18 59165543 intergenic variant G/A snv 0.21 2
rs10783615
HOXC12 ; LOC105369775
12 53955989 intron variant G/A snv 0.71 2
rs10856789 2 19581401 intergenic variant T/A;C snv 2
rs10912872 1 171387110 intergenic variant G/T snv 0.38 2
rs10958852
PTPRD
9 10060843 intron variant C/T snv 4.5E-04 2
rs10991437
CT70
9 104973639 intron variant C/A snv 9.0E-02 2
rs11019935 11 88441800 intergenic variant C/A;T snv 2
rs111645190 19 40855903 intron variant G/A snv 4.2E-02 2
rs111825958
CYP2F2P
19 40825304 intron variant C/A snv 3.5E-02 2
rs112000748 4 123994124 intergenic variant C/T snv 0.12 2
rs112226039 4 188259805 intergenic variant G/A snv 0.18 2
rs11231693
MACROD1 ; FLRT1
11 64095140 intron variant G/A snv 0.11 2
rs112364629
MYRIP
3 39950732 intron variant A/G snv 3.6E-02 2
rs112827279
LOC102724092
X 15234130 downstream gene variant C/A snv 4.1E-02 2
rs112960054
LPXN
11 58564369 intron variant C/G snv 4.0E-02 2