Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 20
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 12
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs6059655
RALY
0.790 0.080 20 34077942 intron variant A/G snv 0.95 10
rs769449
APOE
0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 8
rs71508903
ARID5B
0.807 0.160 10 62020112 intron variant C/T snv 0.15 7
rs10774624
LINC02356
0.882 0.160 12 111395984 intron variant G/A snv 0.67 5
rs1393350
LOC107984363 ; TYR
0.851 0.160 11 89277878 intron variant G/A snv 0.17 5
rs251464
PPARGC1B
0.851 0.080 5 149816671 intron variant G/C snv 0.36 5
rs10876864
IKZF4
0.882 0.120 12 56007301 upstream gene variant G/A snv 0.50 4
rs11203203
UBASH3A
0.807 0.240 21 42416077 intron variant G/A snv 0.28 4
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 4
rs301807
RERE-AS1 ; RERE
0.925 0.080 1 8424763 intron variant A/G;T snv 4
rs4766578
ATXN2
0.851 0.200 12 111466567 intron variant T/A snv 0.66 4
rs706779
IL2RA
0.827 0.160 10 6056861 intron variant T/C snv 0.48 4
rs968567
FADS2 ; FADS1
0.851 0.240 11 61828092 intron variant C/T snv 0.11 4
rs1701704
LOC105369781 ; IKZF4
0.851 0.200 12 56018703 intron variant T/G snv 0.25 3
rs301819
RERE
0.882 0.120 1 8441726 intron variant A/G;T snv 3
rs4268748
DEF8
0.925 0.080 16 89960104 intron variant T/C snv 0.30 3
rs10484554
LOC112267902 ; HLA-B
0.807 0.200 6 31306778 intron variant C/T snv 0.12 2
rs11079035
RAB5C
1.000 0.040 17 42136994 intron variant G/A snv 0.29 2
rs11593576
ZMIZ1
0.925 0.040 10 79256139 intron variant C/T snv 0.29 2
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 2
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 2