Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16917546
LOC105378327 ; ZNF365
0.851 0.040 10 62637778 intron variant T/C snv 0.29 4
rs10995240
LOC105378327 ; ZNF365
10 62628871 intron variant G/C snv 0.29 2
rs12413946
ZNF365
10 62671446 non coding transcript exon variant T/C snv 6.2E-02 2