Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6763931
ZBTB38
0.925 0.080 3 141383991 intron variant G/A snv 0.54 2
rs6937121
ADGRG6
6 142385996 intron variant T/G snv 0.47 2
rs724577
LCORL
4 17991787 intron variant A/C snv 0.71 2
rs750460
LOXL1
1.000 0.040 15 73949165 intron variant G/A;T snv 2
rs7753012
ADGRG6
6 142424746 intron variant T/G snv 0.50 2
rs7759938
LIN28B-AS1
0.925 0.120 6 104931079 intron variant C/T snv 0.62 2
rs879882
POU5F1
1.000 0.160 6 31171675 intron variant T/C;G snv 2
rs9391253
LIN28B-AS1
6 104919741 intron variant A/T snv 0.29 2
rs972982
ADGRG6
6 142345724 intron variant T/C snv 0.44 2
rs10010325
TET2 ; TET2-AS1
1.000 0.040 4 105185196 intron variant C/A;G;T snv 1
rs10037512
MEF2C-AS1
5 89058858 intron variant T/A;C snv 1
rs10058074
MIR3936HG
5 132350453 intron variant G/A snv 0.31 1
rs10152591
DRAIC ; LOC107984788
15 69755818 intron variant A/C snv 9.8E-02 1
rs10187066
ZNF142
2 218650036 intron variant A/G snv 0.45 1
rs1029534
JAZF1
7 28149464 intron variant T/C;G snv 1
rs10401193
GATAD2A
19 19480257 intron variant A/G snv 0.19 1
rs10512248
PTCH1
0.925 0.120 9 95497421 intron variant T/A;G snv 1
rs10513137
ZBTB38
3 141424588 intron variant G/A;C snv 1
rs1074683
PXMP4
20 33716847 intron variant C/G snv 0.24 1
rs10770705
SLCO1C1
12 20704533 intron variant A/C snv 0.70 1
rs10838708
PSMC3
11 47419962 intron variant G/A snv 0.39 1
rs10838798
PTPRJ
11 48069751 intron variant T/G snv 0.56 1
rs10838801
PTPRJ
11 48076728 intron variant G/A snv 0.56 1
rs10843164
CCDC91
12 28416781 intron variant T/C snv 0.22 1
rs10859563
LOC101928731 ; CRADD
12 93726563 intron variant C/G snv 0.40 1