Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs45446698
CYP3A7-CYP3A51P ; CYP3A7 ; ZSCAN25
0.807 0.120 7 99735325 upstream gene variant T/G snv 2.7E-02 3
rs1818782
DAB2 ; C9
5 39424526 intron variant A/C snv 0.56 3
rs10283100
ENPP2
8 119583783 missense variant A/G;T snv 0.96 3
rs798489
GNA12 ; AMZ1
7 2762169 splice donor variant C/T snv 0.20 3
rs1042725
HMGA2
0.882 0.080 12 65964567 3 prime UTR variant C/T snv 0.48 3
rs2928148
INO80
15 41109352 intron variant G/A snv 0.44 3
rs2168101
LMO1 ; LOC105376536
0.827 0.200 11 8233861 intron variant C/A snv 0.24 3
rs7076938
LOC105378493
10 114029616 intergenic variant C/T snv 0.69 3
rs2229742
NRIP1
21 14966851 missense variant G/C snv 7.9E-02 7.1E-02 3
rs72656010
PLAG1 ; CHCHD7
8 56209656 intron variant T/C snv 0.10 3
rs2292626
PLEKHA1
0.925 0.120 10 122427198 intron variant C/T snv 0.46 3
rs11545169
PSMD2
3 184302754 missense variant G/T snv 0.13 0.11 3
rs670523
RIT1
1.000 0.040 1 155908941 intron variant A/G snv 0.48 3
rs9379084
RREB1
0.882 0.160 6 7231610 missense variant G/A snv 0.11 8.9E-02 3
rs2189234
TET2
1.000 0.040 4 105154341 intron variant T/G snv 0.62 3
rs6533183
TET2-AS1 ; TET2
4 105212027 intron variant C/T snv 0.61 3
rs147110934
ZNF628
19 55482069 missense variant G/T snv 1.4E-02 1.5E-02 3
rs12446550 16 28532060 downstream gene variant G/A snv 0.36 2
rs2428362 17 7276955 upstream gene variant C/A;T snv 2
rs28530618 20 32687779 intron variant A/C;G snv 2
rs2908279 1.000 0.080 7 44135258 downstream gene variant T/G snv 0.59 2
rs6925689 6 126544738 intron variant T/C snv 0.45 2
rs7742369 6 34197944 TF binding site variant A/G snv 0.30 2
rs7744700 6 53484603 regulatory region variant T/A;C snv 2
rs7968682 12 65978100 intergenic variant G/T snv 0.56 2