Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4926499 | 1 | 248861710 | intron variant | G/C | snv | 0.87 | 1 | ||||
rs434578 | 6 | 159272188 | downstream gene variant | C/T | snv | 0.86 | 1 | ||||
rs1764975 | 20 | 4120643 | upstream gene variant | T/A | snv | 0.85 | 1 | ||||
rs2999159 | 1 | 112688136 | intron variant | A/G | snv | 0.85 | 4 | ||||
rs2014912 | 4 | 85794517 | intron variant | T/C | snv | 0.84 | 1 | ||||
rs912434 | 13 | 46615793 | intron variant | G/T | snv | 0.84 | 1 | ||||
rs2480171 | 13 | 20985719 | intron variant | T/C | snv | 0.84 | 1 | ||||
rs1489486 | 2 | 178820256 | intron variant | A/G | snv | 0.83 | 1 | ||||
rs2469997 | 8 | 119341027 | intergenic variant | G/C | snv | 0.83 | 2 | ||||
rs964184 | 0.716 | 0.440 | 11 | 116778201 | 3 prime UTR variant | G/C | snv | 0.82 | 47 | ||
rs476636 | 11 | 120455568 | intron variant | G/A | snv | 0.82 | 1 | ||||
rs4335411 | 1.000 | 1 | 248897507 | regulatory region variant | G/A | snv | 0.82 | 3 | |||
rs9872857 | 3 | 186489773 | intron variant | A/T | snv | 0.82 | 1 | ||||
rs284844 | 10 | 102794772 | intron variant | A/G | snv | 0.82 | 3 | ||||
rs6062302 | 0.882 | 0.040 | 20 | 63689615 | synonymous variant | T/C | snv | 0.74 | 0.81 | 4 | |
rs7555285 | 1 | 209797010 | intron variant | G/C | snv | 0.81 | 1 | ||||
rs1257310 | 14 | 99344090 | intergenic variant | C/A | snv | 0.81 | 1 | ||||
rs1882289 | 3 | 114742361 | intron variant | G/A | snv | 0.81 | 1 | ||||
rs7158754 | 14 | 100117012 | intron variant | A/G | snv | 0.81 | 1 | ||||
rs2920899 | 2 | 55052545 | intron variant | G/T | snv | 0.81 | 1 | ||||
rs4143175 | 12 | 67388617 | regulatory region variant | T/C | snv | 0.80 | 1 | ||||
rs11187142 | 10 | 92708928 | downstream gene variant | T/C | snv | 0.80 | 1 | ||||
rs42398 | 5 | 96784751 | intron variant | C/T | snv | 0.80 | 1 | ||||
rs261332 | 0.851 | 0.120 | 15 | 58435126 | non coding transcript exon variant | A/G | snv | 0.80 | 20 | ||
rs4913007 | 5 | 144846912 | intergenic variant | C/T | snv | 0.80 | 1 |