Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6846071 | 4 | 101481058 | intron variant | T/G | snv | 0.15 | 1 | ||||
rs6951245 | 7 | 1018557 | intron variant | G/A | snv | 0.12 | 2 | ||||
rs771767 | 1.000 | 0.080 | 3 | 102029794 | regulatory region variant | A/G | snv | 0.70 | 2 | ||
rs9284725 | 2 | 102128394 | intron variant | C/A;T | snv | 0.82 | 1 | ||||
rs4141632 | 2 | 102140679 | intron variant | A/G;T | snv | 1 | |||||
rs10745954 | 12 | 103089316 | intron variant | A/G | snv | 0.60 | 1 | ||||
rs10778213 | 12 | 103101373 | intron variant | T/C | snv | 0.57 | 1 | ||||
rs4764725 | 12 | 103118536 | intron variant | T/C | snv | 0.56 | 1 | ||||
rs10778215 | 12 | 103143488 | intron variant | T/A;G | snv | 2 | |||||
rs1529711 | 1.000 | 0.080 | 19 | 10912758 | intron variant | C/T | snv | 0.13 | 3 | ||
rs629301 | 0.851 | 0.120 | 1 | 109275684 | 3 prime UTR variant | G/T | snv | 0.74 | 19 | ||
rs646776 | 0.752 | 0.240 | 1 | 109275908 | downstream gene variant | C/T | snv | 0.74 | 10 | ||
rs10744775 | 12 | 111658411 | intron variant | T/C | snv | 0.44 | 2 | ||||
rs10255299 | 7 | 111887504 | intron variant | G/A | snv | 0.11 | 1 | ||||
rs1834481 | 0.882 | 0.160 | 11 | 112153104 | non coding transcript exon variant | C/G | snv | 0.16 | 1 | ||
rs2250417 | 1.000 | 0.080 | 11 | 112214593 | intron variant | T/C | snv | 0.44 | 3 | ||
rs2285810 | 12 | 112261736 | non coding transcript exon variant | T/C | snv | 0.45 | 2 | ||||
rs6761276 | 2 | 113074735 | missense variant | T/C | snv | 0.56 | 0.57 | 1 | |||
rs6743376 | 2 | 113074756 | missense variant | C/A | snv | 0.69 | 0.69 | 1 | |||
rs12711751 | 2 | 113080188 | downstream gene variant | T/G | snv | 0.61 | 2 | ||||
rs13409360 | 2 | 113080525 | downstream gene variant | G/A | snv | 0.38 | 2 | ||||
rs13409371 | 2 | 113080568 | downstream gene variant | G/A;C;T | snv | 1 | |||||
rs6734238 | 1.000 | 0.080 | 2 | 113083453 | upstream gene variant | A/G | snv | 0.39 | 5 | ||
rs3822857 | 6 | 115992768 | intron variant | G/A;C | snv | 3 | |||||
rs12202641 | 6 | 115993471 | intron variant | C/A;T | snv | 1 |