Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2283487 0.925 0.120 16 3919885 intergenic variant A/C;G snv 2
rs2363632 0.925 0.120 12 52963551 intergenic variant T/G snv 7.7E-02 2
rs2872615 0.925 0.120 17 9011376 intergenic variant T/C snv 0.23 2
rs287982 0.925 0.120 2 9832313 regulatory region variant C/T snv 0.70 2
rs3815854 0.925 0.120 2 219804017 intergenic variant C/T snv 0.51 2
rs4901118 0.925 0.120 14 51389391 upstream gene variant G/A snv 0.62 2
rs6129653 0.925 0.120 20 40646963 regulatory region variant T/A;C snv 2
rs6540559 0.925 0.120 1 209808680 upstream gene variant G/A snv 0.28 2
rs6734545 0.925 0.120 2 219789274 intergenic variant C/A snv 1.6E-02 2
rs7148069 0.925 0.120 14 51372927 intron variant C/T snv 0.32 2
rs75477785 0.925 0.120 1 209811125 upstream gene variant T/G snv 3.9E-02 2
rs7554547 0.925 0.120 1 11913831 non coding transcript exon variant A/G;T snv 2
rs77866552 0.925 0.120 2 232687954 regulatory region variant G/A;C snv 1.4E-03 2
rs7871395 0.925 0.120 9 89594672 intron variant C/T snv 0.24 2
rs8049367 0.851 0.240 16 3930444 downstream gene variant T/C snv 0.37 2
rs908822 0.925 0.120 4 123985102 regulatory region variant C/A;T snv 2
rs9381107 0.925 0.120 6 9469005 intergenic variant G/A snv 0.17 2
rs9545308 0.925 0.120 13 80065270 intron variant G/T snv 0.21 2
rs481931
ABCA4
0.882 0.120 1 94104460 intron variant G/T snv 0.32 2
rs11072494
ARID3B
0.925 0.120 15 74596822 3 prime UTR variant C/G;T snv 2
rs6740960
C2orf91
0.925 0.120 2 41954539 intron variant A/T snv 0.61 2
rs7017252
CCDC26
0.925 0.120 8 128938598 intron variant C/T snv 0.32 2
rs68092024
CMSS1 ; FILIP1L
0.925 0.120 3 99972678 intron variant C/T snv 0.68 2
rs1038294
COL8A1
0.925 0.120 3 99784884 intron variant A/G snv 0.82 2
rs7552
CYRIA
0.882 0.120 2 16552660 splice region variant A/G snv 0.44 2