Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72973711
ZNF516
18 76360290 3 prime UTR variant A/T snv 4.8E-02 1
rs28633718
ZNF423
16 49850619 intron variant C/A;G snv 1
rs4703890
ZNF366
5 72452797 intron variant G/A snv 0.85 1
rs10995249
ZNF365 ; LOC105378327
10 62637156 intron variant C/T snv 0.29 1
rs1474419
ZNF316
7 6652974 missense variant T/C;G snv 1
rs118092853
ZNF235
19 44285734 intron variant G/A snv 4.3E-02 1
rs58434384
ZNF101
19 19675290 intron variant A/G snv 0.12 1
rs7832219
ZFPM2-AS1 ; ZFPM2
8 105566749 intron variant T/C snv 0.31 1
rs1350723
ZFPM2
8 105218944 intron variant G/A snv 0.69 1
rs4782371
ZFPM1
1.000 0.040 16 88502423 intron variant T/A;G snv 2
rs10273974
ZC3HAV1
7 139050766 intron variant A/C snv 0.48 1
rs73715668
ZC3H3
8 143544551 non coding transcript exon variant G/C snv 0.18 1
rs238914
ZBTB16
11 114113387 intron variant C/A snv 0.45 5
rs2846630
ZBTB16
11 114086475 intron variant G/A snv 0.35 5
rs238913
ZBTB16
11 114113767 intron variant A/G snv 0.46 1
rs1689791
YPEL5P1 ; LINC01344
1 182182774 non coding transcript exon variant A/G snv 0.32 1
rs878825
YDJC
22 21627960 upstream gene variant T/C snv 0.32 3
rs12787996
YAP1
11 102186337 non coding transcript exon variant C/A snv 0.31 1
rs188192
XPO6
16 28120189 intron variant C/A;T snv 0.30 1
rs11075747
WWP2
16 69906458 intron variant G/A snv 0.47 1
rs7025371
WDR31
9 113323542 intron variant A/G snv 0.57 1
rs28434172
WDR26
1 224426923 intron variant C/T snv 0.18 1
rs34687215
WDR26
1 224394506 intron variant TT/-;T;TTT;TTTTT;TTTTTT;TTTTTTT delins 0.19 1
rs4272720
VSTM4
10 49055156 intron variant A/G snv 0.29 2
rs17011726
VSTM4
10 49056159 intron variant C/G snv 0.18 1