Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7524102 0.882 0.160 1 22371954 intergenic variant A/G snv 0.21 5
rs4730775
WNT2
0.851 0.200 7 117277064 3 prime UTR variant C/T snv 0.41 4
rs10809650 0.925 0.120 9 1202371 intergenic variant A/G snv 0.26 2
rs2179367 0.925 0.120 6 149441401 regulatory region variant A/G snv 0.50 2
rs4932194 0.925 0.120 15 88702008 regulatory region variant A/C;G;T snv 2
rs6519955 0.925 0.120 22 46025962 regulatory region variant G/T snv 0.50 2
rs8124695 0.925 0.120 20 40399796 intergenic variant C/A;T snv 2
rs4789939
CEP295NL ; TIMP2
0.925 0.120 17 78885621 intron variant T/A;C snv 2
rs11672517
DUXA
0.925 0.120 19 57166826 intron variant G/A snv 0.24 2
rs611744
EIF3E
0.925 0.120 8 108215779 intron variant A/G;T snv 2
rs16879765
EPDR1 ; SFRP4
0.925 0.120 7 37949493 intron variant C/T snv 0.13 2
rs2912522
LINC01592
0.925 0.120 8 69080145 intron variant G/A snv 0.73 2
rs11666105
DHDH
1.000 0.120 19 48942560 missense variant T/C snv 0.28; 4.0E-06 0.34 1
rs2270941
DHDH
1.000 0.120 19 48935106 missense variant G/A snv 0.34 0.40 1