Disease: Alcohol consumption
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13149993 4 80237391 regulatory region variant G/A;C snv 6
rs17035646
CASZ1
1 10736490 intron variant G/A;T snv 6
rs2643826 3 27521497 upstream gene variant C/T snv 0.56 6
rs35444 12 115114632 intergenic variant A/G snv 0.38 6
rs62434129
PLEKHG1
6 150687701 intron variant A/G;T snv 8.8E-02 6
rs7209400
LOC102724596
1.000 0.040 17 49372695 intron variant C/T snv 0.47 6
rs9292468 5 32818967 intergenic variant T/A;C snv 6
rs10184428 2 164155317 intron variant C/A;G snv 5
rs11513729 1.000 0.080 12 111835695 downstream gene variant C/T snv 0.29 5
rs11725969
GUCY1A1
4 155705436 intron variant C/T snv 0.24 5
rs12978472
INSR
19 7257979 intron variant C/G;T snv 5
rs13209747 6 126794309 intron variant C/G;T snv 0.36 5
rs1573643
FURIN
15 90877743 intron variant T/C snv 0.33 5
rs1813353
CACNB2
10 18418519 intron variant T/C snv 0.29 5
rs1894400
FES
15 90885725 intron variant C/T snv 0.28 5
rs2004776
AGT
1 230712956 intron variant C/G;T snv 5
rs2013002 12 111762346 intron variant T/A;C snv 5
rs35441 12 115115310 intergenic variant C/T snv 0.40 5
rs35443 12 115115073 intergenic variant G/C snv 0.40 5
rs4980389
LSP1
11 1871355 5 prime UTR variant G/A snv 0.35 5
rs6108787 20 10986566 intron variant T/G snv 0.46 5
rs7125196
LOC105369329
11 61505093 intron variant T/C snv 0.16 5
rs7953257
HECTD4
12 112246417 intron variant A/G;T snv 0.71 5
rs10750766 11 65706327 regulatory region variant C/A snv 0.60 4
rs11105352
ATP2B1
12 89632685 intron variant G/A snv 0.14 4