Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34667100 12 6185569 intergenic variant T/C snv 0.41 1
rs35115423 9 124425950 intergenic variant GT/- delins 1
rs370869951 1 150355421 downstream gene variant AAAA/-;A;AAA;AAAAA;AAAAAA;AAAAAAAAAAAAA delins 1
rs373518068 2 226469439 intergenic variant ATAT/-;AT;ATATAT;ATATATAT delins 1
rs397969 17 19900934 upstream gene variant T/C snv 0.41 1
rs409801 9 4744743 intron variant T/C snv 0.38 1
rs409950 9 4763368 downstream gene variant C/A;G snv 1
rs4670779 2 37817201 non coding transcript exon variant C/T snv 0.23 1
rs4711890 6 47638976 intergenic variant C/G snv 0.27 1
rs4846217 1 10391742 upstream gene variant C/T snv 0.14 1
rs497453 19 56128492 upstream gene variant A/C;T snv 0.95 1
rs61542570 17 29380621 intron variant AAA/-;A;AA;AAAA;AAAAAAAAA delins 1
rs6445967 3 58296849 downstream gene variant T/C snv 0.38 1
rs6556471 5 160171257 intergenic variant T/C snv 0.70 1
rs670179 13 70662475 intergenic variant T/A snv 0.52 1
rs6735923 2 159913077 intergenic variant T/C snv 0.42 1
rs6779488 3 12229161 intergenic variant A/G snv 0.12 1
rs7149242 14 100693079 intergenic variant T/G snv 0.62 1
rs71633359 4 87262668 intron variant T/C snv 1
rs7178196 15 56786080 intron variant G/A;T snv 1
rs7249921 19 35170884 downstream gene variant C/T snv 0.36 1
rs74340846 1 30769039 intergenic variant G/T snv 5.6E-03 1
rs74887316 4 52182445 intergenic variant C/T snv 7.5E-03 1
rs75140056 6 29640407 upstream gene variant -/A;AT ins 0.60 1
rs7665147 4 56901161 intergenic variant T/A;G snv 1