Disease: Severe myopia
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10824518
KCNMA1
0.882 0.040 10 77303784 intron variant T/A;C snv 3
rs12423791
IGF1
0.925 0.040 12 102465050 intron variant G/C snv 2.8E-02 5
rs12716080
CTNND2
0.882 0.040 5 11166836 intron variant G/T snv 0.39 3
rs13382811
ZEB2
0.882 0.040 2 144466053 intron variant C/T snv 0.21 4
rs1635529
COL2A1
0.925 0.040 12 48001319 intron variant T/G snv 0.78 2
rs2973644
FGF10
0.925 0.040 5 44384081 intron variant C/A;T snv 2
rs3026393
ELP4 ; PAX6
0.925 0.040 11 31790667 intron variant A/C;G;T snv 0.48; 8.0E-06; 7.6E-05 2
rs339501
FGF10
0.925 0.040 5 44365531 intron variant C/T snv 0.94 2
rs5742632
LINC02456 ; IGF1
0.851 0.120 12 102462696 intron variant A/G snv 0.26 4
rs577948
MIR100HG
0.882 0.040 11 122159482 intron variant A/G snv 0.33 3
rs6469937
SNTB1
0.882 0.040 8 120598198 intron variant G/A snv 0.48 3
rs6885224
CTNND2
0.882 0.040 5 11169833 intron variant C/A;T snv 3
rs7839488
SNTB1
0.882 0.040 8 120550178 intron variant G/A snv 0.47 4
rs79002828
FGF10
0.925 0.040 5 44318015 intron variant A/G snv 9.6E-03 2
rs8027411
ANKRD34C-AS1
0.882 0.040 15 79168687 intron variant G/T snv 0.52 4
rs9318086
MIPEP
0.882 0.040 13 23858328 intron variant A/G snv 0.55 3
rs10034228 0.882 0.040 4 111690594 intergenic variant T/C snv 0.32 3
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
rs4373767 0.882 0.040 1 219586340 regulatory region variant C/T snv 0.32 4
rs1644731
RDH8
0.925 0.040 19 10021323 missense variant T/A;C snv 4.0E-06; 0.52 2
rs747797174
GOLGA6A
0.925 0.040 15 74070978 missense variant C/A;G;T snv 1.2E-05 2
rs10860860
HELLPAR ; LINC02456
0.925 0.040 12 102387055 non coding transcript exon variant A/T snv 0.28 2
rs2946834
LINC02456 ; HELLPAR
0.807 0.200 12 102394036 non coding transcript exon variant A/G snv 0.63 7
rs644242
PAX6
0.882 0.040 11 31791253 non coding transcript exon variant C/A;G snv 3