Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10033900
CFI
0.807 0.040 4 109737911 intron variant T/C snv 0.54 7
rs524952 0.827 0.040 15 34713685 intergenic variant T/A snv 0.50 6
rs569681869
COL4A4
0.925 0.040 2 227059468 missense variant C/G snv 7.2E-05 3.5E-05 6
rs634990 0.827 0.040 15 34713872 intergenic variant T/C snv 0.48 6
rs12423791
IGF1
0.925 0.040 12 102465050 intron variant G/C snv 2.8E-02 5
rs2274755
MMP9
0.882 0.040 20 46011053 splice region variant G/T snv 0.15 0.15 5
rs3138141
RDH5 ; BLOC1S1-RDH5
0.827 0.040 12 55721994 3 prime UTR variant C/A snv 0.19 0.16 5
rs533297350
COL4A4
1.000 0.040 2 227010441 missense variant C/T snv 7.2E-05 3.5E-05 5
rs13382811
ZEB2
0.882 0.040 2 144466053 intron variant C/T snv 0.21 4
rs397515624
CRYAA ; LOC107987300
0.851 0.040 21 43169133 missense variant C/T snv 4.0E-06 4
rs4373767 0.882 0.040 1 219586340 regulatory region variant C/T snv 0.32 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
rs9330813
WNT7B
1.000 0.040 22 45968281 intron variant G/A;C snv 4
rs10034228 0.882 0.040 4 111690594 intergenic variant T/C snv 0.32 3
rs10453441
WNT7B
1.000 0.040 22 45967859 intron variant A/G snv 0.40 3
rs10500355
RBFOX1
0.925 0.040 16 7409346 intron variant T/A snv 0.29 3
rs10824518
KCNMA1
0.882 0.040 10 77303784 intron variant T/A;C snv 3
rs12193446
LAMA2 ; LOC102723409
0.925 0.040 6 129498893 intron variant A/G snv 6.4E-02 3
rs12716080
CTNND2
0.882 0.040 5 11166836 intron variant G/T snv 0.39 3
rs577948
MIR100HG
0.882 0.040 11 122159482 intron variant A/G snv 0.33 3
rs644242
PAX6
0.882 0.040 11 31791253 non coding transcript exon variant C/A;G snv 3
rs6469937
SNTB1
0.882 0.040 8 120598198 intron variant G/A snv 0.48 3
rs662702
PAX6 ; ELP4
0.882 0.040 11 31787522 3 prime UTR variant C/T snv 0.15 3
rs6885224
CTNND2
0.882 0.040 5 11169833 intron variant C/A;T snv 3