Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104893768
RHO
0.807 0.080 3 129528801 missense variant C/A snv 11
rs29001566
RHO
0.807 0.080 3 129533711 missense variant C/A;G;T snv 10
rs104893775
RHO
0.807 0.160 3 129530917 missense variant C/T snv 7
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
rs7084402 0.925 0.040 10 58505644 intergenic variant A/G snv 0.51 4
rs8027411
ANKRD34C-AS1
0.882 0.040 15 79168687 intron variant G/T snv 0.52 4
rs17183295
MYO1D
1.000 17 32751254 intron variant C/T snv 0.14 4
rs17648524
RBFOX1
0.882 0.040 16 7409682 intron variant G/C snv 0.29 4
rs7839488
SNTB1
0.882 0.040 8 120550178 intron variant G/A snv 0.47 4
rs13382811
ZEB2
0.882 0.040 2 144466053 intron variant C/T snv 0.21 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
rs1254319
C14orf39
1.000 14 60437039 missense variant G/A snv 0.35 0.36 3
rs7744813
KCNQ5
0.925 0.040 6 72933566 intron variant C/A snv 0.66 3
rs10500355
RBFOX1
0.925 0.040 16 7409346 intron variant T/A snv 0.29 3
rs7829127
ZMAT4
0.925 0.040 8 40868875 intron variant A/G snv 0.22 3
rs10882165 1.000 10 93164567 intergenic variant A/T snv 0.39 2
rs11073060 1.000 0.040 15 34697650 intergenic variant C/A snv 0.41 2
rs1960445 1.000 4 81009660 intergenic variant C/T snv 0.81 2
rs235770 1.000 20 6781118 downstream gene variant T/C snv 0.71 2
rs4793501 1.000 17 70722593 intergenic variant C/T snv 0.64 2
rs7837791 1.000 8 59266527 intergenic variant G/A;T snv 2