Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs766406 6 26319360 downstream gene variant G/T snv 0.74 1
rs139909
TNRC6B
22 40301577 intron variant C/T snv 0.74 1
rs2707450
LCORL
4 17940937 intron variant C/T snv 0.73 1
rs537160
CYP21A2 ; CFB
0.882 0.240 6 31948623 intron variant A/G snv 0.73 1
rs1801222
CUBN
0.925 0.160 10 17114152 missense variant A/G snv 0.73 0.72 2
rs395962
LIN28B
6 104949543 intron variant T/G snv 0.72 1
rs3103267
DIS3L2
2 232123872 intron variant A/C snv 0.72 1
rs2724475
LCORL
4 17944809 intron variant T/C snv 0.71 1
rs724577
LCORL
4 17991787 intron variant A/C snv 0.71 2
rs153750 5 171754233 intergenic variant T/G snv 0.71 1
rs1787200
DYM
18 49061284 intron variant G/A snv 0.71 1
rs1759645 6 34227089 TF binding site variant C/T snv 0.71 1
rs2341459
CAMKMT
2 44541063 intron variant T/C snv 0.70 1
rs10770705
SLCO1C1
12 20704533 intron variant A/C snv 0.70 1
rs925098
LCORL
4 17918188 intron variant G/A snv 0.70 1
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 1
rs314263
LIN28B
6 104944870 intron variant C/T snv 0.69 1
rs6918981 6 34270737 intron variant G/A snv 0.69 1
rs2854160 17 63899888 upstream gene variant T/C snv 0.69 1
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 1
rs2280470
ACAN
15 88852395 intron variant A/G snv 0.68 1
rs1950500 14 24361644 upstream gene variant T/C snv 0.68 1
rs9969804
IPPK
9 92666838 intron variant A/C snv 0.68 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24