Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs497453 19 56128492 upstream gene variant A/C;T snv 0.95 1
rs10661645
NAA25
12 112086916 intron variant -/GAG;GGAG delins 0.95 1
rs9704108
IFITM2
11 308065 5 prime UTR variant T/C snv 0.95 1
rs4543312
FABP6
5 160193485 intron variant T/C snv 0.93 1
rs4148441
ABCC4
13 95245953 intron variant A/G snv 0.91 1
rs4148435
ABCC4
13 95247462 intron variant C/A snv 0.91 1
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 4
rs7788849
NRF1
7 129642078 intron variant C/A;G snv 0.90 1
rs2836441
ERG
21 38498386 5 prime UTR variant G/A snv 0.87 0.89 1
rs625132
EHD3
2 31259434 intron variant A/G snv 0.82 1
rs655641
PICALM
11 86020243 intron variant C/G snv 0.82 1
rs7641175
TBC1D5
3 18269920 intron variant G/A snv 0.81 3
rs10132160
RCOR1
14 102591686 upstream gene variant A/G snv 0.80 1
rs3844535
STON2
14 81418171 non coding transcript exon variant A/G snv 0.78 1
rs10914144
DNM3
1 171980610 intron variant T/C snv 0.78 2
rs655029
EHD3
2 31254972 intron variant G/A snv 0.78 3
rs7529925
LINC01221
1 199038079 intron variant C/T snv 0.77 3
rs10199109
LOC105373583
2 120236957 upstream gene variant G/T snv 0.75 1
rs3731211
CDKN2A
9 21986848 intron variant T/A snv 0.74 7
rs210142
GGNBP1 ; BAK1
0.925 0.120 6 33579060 intron variant T/C snv 0.74 3
rs210143
GGNBP1 ; BAK1
0.827 0.160 6 33579153 intron variant T/C snv 0.74 5
rs477895
BAD ; GPR137
11 64281440 intron variant C/T snv 0.74 1
rs210134
BAK1 ; GGNBP1
1.000 0.120 6 33572432 intron variant A/G snv 0.72 1
rs853195
DUSP14
17 37488149 upstream gene variant C/A snv 0.71 1
rs7550918
GCSAML
1 247512257 intron variant C/T snv 0.70 1