Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
rs10475992
FBXW11
5 171908289 intron variant C/T snv 0.42 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
rs10804515
ZBTB20
3 114983210 intron variant A/G snv 0.60 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
rs10863936
DTL
1 212064456 intron variant G/A snv 0.59 1
rs10874746
DIPK1A
1 92858414 intron variant T/A;C snv 1
rs10906982
ADAMTSL3
15 83899406 intron variant T/A snv 0.63 1
rs10935120
CEP63
3 134514250 intron variant A/G snv 0.63 1
rs10948222
SUPT3H
6 45276678 intron variant T/C snv 0.40 1
rs10958476
PLAG1
8 56183249 intron variant T/C snv 0.16 1