Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs35874463
SMAD3
0.827 0.120 15 67165360 missense variant A/G snv 4.0E-02 3.4E-02 7
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 6
rs2294214
CASC15
0.882 0.040 6 22056694 splice region variant A/C;T snv 6
rs76895963
CCND2-AS1 ; CCND2
1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 6
rs7740107
L3MBTL3
1.000 0.080 6 130053316 intron variant T/A;G snv 6
rs1142
SRPK2
0.851 0.040 7 105115879 intron variant C/T snv 0.31 6
rs10059884 5 32832368 regulatory region variant C/A;T snv 5
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 5
rs17391694 0.882 0.120 1 78157942 regulatory region variant C/T snv 7.8E-02 5
rs1884897 20 6632185 regulatory region variant A/G;T snv 5
rs9292468 5 32818967 intergenic variant T/A;C snv 5
rs72755233
ADAMTS17
1.000 0.080 15 100152748 missense variant G/A;T snv 7.1E-02; 3.2E-05 5
rs10189857
BCL11A
1.000 0.080 2 60486100 intron variant A/G snv 0.42 5
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 5
rs2812208
DLEU1
13 50132951 intron variant G/A;C snv 5
rs1129555
GPAM
10 112150963 3 prime UTR variant A/G snv 0.71 5
rs1812175
HHIP-AS1 ; HHIP
4 144653692 intron variant A/G snv 0.79 5
rs1167827
HIP1
7 75533848 3 prime UTR variant G/A snv 0.37 5
rs7801581
HOXA11-AS ; HOXA11
7 27184152 intron variant C/T snv 0.24 5
rs6569648
L3MBTL3
1.000 0.080 6 130027974 intron variant C/T snv 0.84 5
rs395962
LIN28B
6 104949543 intron variant T/G snv 0.72 5
rs114165349
LOC101928728 ; ARID1A
1 26695422 intron variant G/C snv 1.7E-02 5
rs7141420
NRXN3
1.000 0.080 14 79433111 intron variant C/T snv 0.56 5
rs5742915
PML
0.925 0.080 15 74044292 missense variant T/C;G snv 0.35; 4.0E-06 5