Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10107630
CCDC26
8 129591389 intron variant C/T snv 0.54 3
rs10164806
ZEB2
2 144435759 intron variant C/T snv 6.7E-02 2
rs10197140
ACOXL
2 110852366 intron variant T/C snv 0.28 3
rs10207392
ACOXL ; MIR4435-2HG
2 111092082 intron variant A/G snv 0.48 1
rs10225965
LOC112268009 ; CDK6
7 92644264 intron variant C/T snv 0.26 1
rs10267576
H2AZ2
7 44831334 intron variant T/C snv 0.35 1
rs10415135
ZBTB7A
19 4061546 intron variant C/T snv 0.23 3
rs10420951 19 18526808 upstream gene variant C/G snv 0.81 2
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs1050828
G6PD
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02 6
rs1053004
STAT3
0.776 0.280 17 42314074 3 prime UTR variant G/A snv 0.48 1
rs10736831
TMEM72-AS1
10 44906863 intron variant G/A snv 0.55 2
rs10751450
ATP2B4
1 203681817 intron variant C/G;T snv 2
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 6
rs10758658
RCL1
9 4856877 intron variant G/A snv 0.15 3
rs10766533
CSRP3 ; CSRP3-AS1
11 19203130 intron variant T/A snv 0.62 4
rs10783487
ATG101
12 52068035 upstream gene variant G/A;T snv 2
rs10849023 12 4223312 intergenic variant C/T snv 0.22 3
rs10923397 1 117708521 regulatory region variant C/T snv 0.14 2
rs10929547
LOC105373411
2 8600592 upstream gene variant C/A snv 0.44 1
rs10947997
CCND3
6 41953503 intron variant G/T snv 0.13 2
rs11031096 11 4139451 upstream gene variant T/C snv 0.47 2
rs11078917 17 39590106 intergenic variant A/C snv 0.56 2
rs11085824
GCDH
19 12890733 upstream gene variant A/G snv 0.31 4
rs11153147
ARMC2
6 108982855 downstream gene variant A/C;G snv 1