Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 9
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 9
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 7
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 6
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 5
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs31489
CLPTM1L
0.763 0.320 5 1342599 intron variant C/A snv 0.41 4
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 4
rs578776
CHRNA3
0.742 0.240 15 78596058 3 prime UTR variant G/A snv 0.39 3
rs8040868
CHRNA3
0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 3
rs1451240 0.925 0.080 8 42691568 intergenic variant A/G snv 0.64 2
rs13273442 0.882 0.080 8 42688874 intergenic variant A/G snv 0.66 1
rs4105144 0.827 0.160 19 40852719 intron variant T/C snv 1
rs6474412 0.925 0.120 8 42695355 upstream gene variant C/T snv 0.64 1
rs848353 1.000 0.080 7 108908603 upstream gene variant A/G snv 0.14 1
rs6484320
BDNF-AS ; BDNF
1.000 0.080 11 27681641 intron variant T/A;G snv 1
rs1317286
CHRNA3
0.925 0.120 15 78603787 intron variant A/G snv 0.30 1
rs6495308
CHRNA3
0.851 0.160 15 78615314 intron variant T/C snv 0.29 1
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 1
rs13280604
CHRNB3 ; LOC105379396
0.851 0.160 8 42704443 5 prime UTR variant G/A snv 0.62 1
rs3733829
EGLN2 ; RAB4B-EGLN2
0.882 0.120 19 40804666 non coding transcript exon variant A/G snv 0.28 1
rs1329650
HECTD2-AS1
0.882 0.080 10 91588363 regulatory region variant G/A;T snv 1
rs4887074
LOC112268142 ; CHRNB4
1.000 0.080 15 78659768 intron variant G/C snv 0.56 1
rs4767364
NAA25
0.807 0.160 12 112083644 intron variant G/A snv 0.45 1
rs880395
PSMA4
1.000 0.080 15 78552014 3 prime UTR variant A/G;T snv 1