Disease: Alcohol consumption
Source: ALL
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 34
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 15
rs7137828
ATXN2
0.763 0.200 12 111494996 intron variant C/A;T snv 15
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs12509595 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 10
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 10
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 9
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 9
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs740746 10 114033028 intergenic variant G/A snv 0.70 8
rs2306363
SIPA1
11 65638129 5 prime UTR variant G/T snv 0.15 7
rs10255839
EVX1
7 27249498 intron variant G/A snv 0.87 6
rs11099097 4 80246155 intergenic variant C/T snv 0.30 6
rs1290784
MECOM
3 169379112 intron variant C/A;T snv 6
rs13125101 4 80253438 TF binding site variant G/A snv 0.24 6
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