Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2844509
SNORD84 ; DDX39B-AS1 ; DDX39B ; ATP6V1G2-DDX39B
0.882 0.160 6 31543147 intron variant A/G snv 0.23 6
rs9267487
ATP6V1G2-DDX39B ; DDX39B ; DDX39B-AS1
1.000 6 31543573 intron variant T/C snv 5.5E-02 4
rs929138
SNORD117 ; DDX39B ; ATP6V1G2-DDX39B
1.000 6 31535921 intron variant T/C snv 0.21 4