Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs6311
HTR2A
0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs806368
CNR1
0.752 0.280 6 88140381 3 prime UTR variant T/C snv 0.19 14
rs2020936
SLC6A4
0.776 0.160 17 30223796 intron variant G/A;C snv 10
rs13280604
CHRNB3 ; LOC105379396
0.851 0.160 8 42704443 5 prime UTR variant G/A snv 0.62 7
rs1451240 0.925 0.080 8 42691568 intergenic variant A/G snv 0.64 4
rs1800498
DRD2
0.882 0.080 11 113420866 intron variant G/A snv 0.44 4