Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10016022
ZNF518B
0.925 0.120 4 10445282 missense variant A/G;T snv 0.74 3
rs10938799
ZNF518B
0.925 0.120 4 10441801 3 prime UTR variant G/A snv 0.21 3
rs12019277
ZNF518B
0.925 0.120 4 10453370 non coding transcript exon variant C/A;T snv 3
rs3217
ZNF518B
0.925 0.120 4 10443026 3 prime UTR variant C/T snv 0.28 3
rs4422413
ZNF518B
0.925 0.120 4 10441760 3 prime UTR variant T/G snv 0.28 3
rs7674156
ZNF518B
0.925 0.120 4 10451139 non coding transcript exon variant G/C snv 0.28 3
rs10516200
WDR1 ; MIR3138
0.925 0.120 4 10080532 intron variant C/A;T snv 3
rs10939710
WDR1
0.925 0.120 4 10115177 intron variant T/C snv 0.30 3
rs11726271
WDR1
0.925 0.120 4 10096568 non coding transcript exon variant G/A;C snv 0.44 3
rs11727087
WDR1
0.925 0.120 4 10094396 intron variant C/T snv 0.35 3
rs11731597
WDR1
0.925 0.120 4 10073861 upstream gene variant C/T snv 0.29 3
rs12498927
WDR1
0.925 0.120 4 10113899 intron variant A/G;T snv 0.51 3
rs12509714
WDR1
0.925 0.120 4 10105467 intron variant C/G snv 0.49 3
rs16868326
WDR1
0.925 0.120 4 10100969 intron variant T/A;C snv 3
rs200251830
WDR1
0.925 0.120 4 10073861 upstream gene variant -/AT delins 3
rs2241468
WDR1
0.925 0.120 4 10112281 intron variant G/A;C snv 3
rs2241470
WDR1
0.925 0.120 4 10082946 intron variant T/G snv 0.31 3
rs2241473
WDR1
0.925 0.120 4 10084325 intron variant G/A snv 0.17 3
rs2241480
WDR1
0.925 0.120 4 10088139 intron variant C/A;T snv 3
rs2241483
WDR1
0.925 0.120 4 10098207 intron variant A/G snv 0.44 3
rs2241486
WDR1
0.925 0.120 4 10099459 intron variant C/A;G snv 3
rs2241488
WDR1
0.925 0.120 4 10099507 intron variant T/C snv 0.16 3
rs3756223
WDR1
0.925 0.120 4 10104173 intron variant T/C snv 0.45 3
rs3756227
WDR1
0.925 0.120 4 10086371 intron variant C/A;G;T snv 3
rs3756230
WDR1
0.925 0.120 4 10082205 intron variant C/G snv 0.18 3