Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 9
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs4665972
SNX17
2 27375230 intron variant T/C snv 0.69 8
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 7
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 6
rs11048456
LOC105369705
1.000 0.080 12 26310149 intron variant C/T snv 0.62 6
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60 6
rs4737010
ANK1
8 41772929 intron variant G/A snv 0.32 6
rs7133378
DNAH10 ; CCDC92
12 123924955 intron variant G/A snv 0.38 6
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 6
rs113542380
THADA
2 43237679 intron variant G/A snv 4.7E-02 5
rs1175550
SMIM1
1 3774964 intron variant A/G snv 0.31 5
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 5
rs2022003
SPTA1
1 158617176 intron variant A/T snv 0.28 5
rs592423 6 139519556 intron variant A/C snv 0.50 5
rs74035509
ZFPM1
16 88500925 intron variant C/T snv 0.10 5
rs766432
BCL11A
0.925 0.080 2 60492835 intron variant C/A snv 0.80 5
rs11021221 11 95575690 intron variant T/A;G snv 4
rs113700287
THRB
3 24293020 intron variant -/GTT delins 4
rs12050884
EIF2AK4
15 40014133 intron variant C/A snv 0.25 4
rs12489828
NT5DC2
3 52532998 intron variant G/T snv 0.51 4
rs1354034
ARHGEF3
3 56815721 intron variant T/C snv 0.49 4
rs159058
NOL4L ; LOC101929698
20 32520305 intron variant A/C;T snv 4