Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16917302
ZNF365
0.851 0.080 10 62501439 intron variant A/C snv 0.18 5
rs10822013
ZNF365
0.851 0.080 10 62492218 intron variant C/T snv 0.42 4
rs10995190
ZNF365
0.882 0.080 10 62518923 intron variant G/A snv 0.16 3
rs7076156
ZNF365 ; LOC105378327
0.925 0.120 10 62655424 missense variant A/C;G snv 0.80 3
rs16917546
LOC105378327 ; ZNF365
0.851 0.040 10 62637778 intron variant T/C snv 0.29 2