Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1985317 9 117530056 intergenic variant C/T snv 0.48 1
rs2028385 12 96423644 intron variant A/G snv 0.19 1
rs2144940 20 23070169 downstream gene variant C/G;T snv 1
rs2567617 20 23068910 downstream gene variant G/A snv 0.88 1
rs2748331 6 71011625 regulatory region variant T/C snv 0.36 1
rs2771051 9 117525430 intergenic variant G/A;T snv 1
rs28496996 18 1952126 intron variant T/G snv 3.1E-02 1
rs28802027 X 155390840 intergenic variant G/T snv 0.11 1
rs3002417 X 39849470 upstream gene variant T/C snv 0.34 1
rs318497 6 2912043 non coding transcript exon variant G/A snv 0.45 1
rs370396210 4 154580036 downstream gene variant -/CA delins 4.2E-05 1
rs467650 5 98633749 intergenic variant T/C snv 0.41 1
rs4696594 4 154497495 intergenic variant G/A snv 0.76 1
rs493014 9 133320327 downstream gene variant T/A;G snv 0.38 1
rs530059570 1 206173141 downstream gene variant G/A snv 6.2E-03 1
rs55899364 17 49981492 intergenic variant C/A;G snv 1
rs59994833 3 183431533 upstream gene variant C/A snv 2.0E-02 1
rs6083037 20 23201922 regulatory region variant A/T snv 0.15 1
rs62187992 2 212677971 intron variant G/A snv 5.1E-02 1
rs6536024 4 154622217 upstream gene variant T/C snv 0.46 1
rs6731933 2 114206140 intergenic variant G/A snv 7.9E-02 1
rs7245232 18 73992717 intron variant G/C snv 0.15 1
rs72705895 1 168603482 regulatory region variant C/A;T snv 5.3E-02 1
rs72708008 1 169508867 downstream gene variant A/G snv 5.7E-02 1
rs73642995 9 26754898 intron variant C/G;T snv 2.6E-03 1