Disease: Refractive Errors
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs524952 0.827 0.040 15 34713685 intergenic variant T/A snv 0.50 6
rs634990 0.827 0.040 15 34713872 intergenic variant T/C snv 0.48 6
rs13382811
ZEB2
0.882 0.040 2 144466053 intron variant C/T snv 0.21 4
rs17648524
RBFOX1
0.882 0.040 16 7409682 intron variant G/C snv 0.29 4
rs4373767 0.882 0.040 1 219586340 regulatory region variant C/T snv 0.32 4
rs7084402 0.925 0.040 10 58505644 intergenic variant A/G snv 0.51 4
rs7839488
SNTB1
0.882 0.040 8 120550178 intron variant G/A snv 0.47 4
rs8027411
ANKRD34C-AS1
0.882 0.040 15 79168687 intron variant G/T snv 0.52 4
rs11073058 1.000 0.040 15 34697425 regulatory region variant G/A;T snv 3
rs1656404 0.925 0.040 2 232515231 regulatory region variant G/A snv 0.18 3
rs17175798
ANKRD34C-AS1
0.925 0.040 15 79171618 intron variant C/A;T snv 3
rs7829127
ZMAT4
0.925 0.040 8 40868875 intron variant A/G snv 0.22 3