Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3745442 | 19 | 54361091 | missense variant | G/C | snv | 0.99 | 1 | ||||
rs370911 | 1 | 162323515 | intron variant | A/G | snv | 0.99 | 6 | ||||
rs830948 | 2 | 169358254 | intron variant | G/A | snv | 0.99 | 3 | ||||
rs556766 | 9 | 35089051 | 3 prime UTR variant | A/C | snv | 1.00 | 0.98 | 1 | |||
rs2321168 | 13 | 33279354 | non coding transcript exon variant | G/A | snv | 0.98 | 4 | ||||
rs891142 | 16 | 56970065 | intron variant | T/C | snv | 0.97 | 1 | ||||
rs567279 | 1 | 66222346 | intron variant | G/T | snv | 0.97 | 4 | ||||
rs891141 | 16 | 56969811 | intron variant | G/T | snv | 0.96 | 1 | ||||
rs231774 | 2 | 203867500 | upstream gene variant | T/A | snv | 0.96 | 1 | ||||
rs11921179 | 3 | 129976195 | intron variant | G/A | snv | 0.96 | 5 | ||||
rs8056298 | 16 | 16142666 | 3 prime UTR variant | T/G | snv | 0.95 | 1 | ||||
rs2072560 | 11 | 116791110 | missense variant | T/C | snv | 0.89 | 0.94 | 5 | |||
rs6589565 | 11 | 116769521 | intron variant | A/G | snv | 0.93 | 5 | ||||
rs7350481 | 0.882 | 0.040 | 11 | 116715567 | regulatory region variant | T/C | snv | 0.93 | 1 | ||
rs2266788 | 0.763 | 0.440 | 11 | 116789970 | 3 prime UTR variant | G/A | snv | 0.93 | 7 | ||
rs4402881 | 3 | 33012839 | intron variant | T/C | snv | 0.93 | 2 | ||||
rs9326246 | 0.925 | 0.040 | 11 | 116741017 | intergenic variant | C/G | snv | 0.93 | 8 | ||
rs2160669 | 1.000 | 0.040 | 11 | 116776891 | 3 prime UTR variant | C/T | snv | 0.92 | 2 | ||
rs662799 | 0.689 | 0.480 | 11 | 116792991 | upstream gene variant | G/A | snv | 0.90 | 6 | ||
rs505151 | 0.732 | 0.360 | 1 | 55063514 | missense variant | G/A | snv | 0.95 | 0.90 | 3 | |
rs4841132 | 8 | 9326086 | non coding transcript exon variant | A/G | snv | 0.89 | 1 | ||||
rs651821 | 0.851 | 0.360 | 11 | 116791863 | 5 prime UTR variant | C/T | snv | 0.88 | 0.89 | 6 | |
rs5072 | 11 | 116836867 | intron variant | A/G | snv | 0.89 | 3 | ||||
rs1461729 | 1.000 | 8 | 9329732 | intron variant | A/G | snv | 0.88 | 3 | |||
rs6601299 | 0.925 | 0.040 | 8 | 9327181 | intron variant | T/C | snv | 0.88 | 2 |