Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2958557 | 8 | 19394168 | intron variant | T/C | snv | 1.00 | 1 | ||||
rs4758675 | 12 | 122207191 | missense variant | C/A;G | snv | 1.00 | 0.99 | 1 | |||
rs370911 | 1 | 162323515 | intron variant | A/G | snv | 0.99 | 6 | ||||
rs7955371 | 12 | 885321 | missense variant | G/C | snv | 1.00 | 0.99 | 1 | |||
rs7100433 | 10 | 133370298 | intron variant | T/C | snv | 0.98 | 3 | ||||
rs2321168 | 13 | 33279354 | non coding transcript exon variant | G/A | snv | 0.98 | 4 | ||||
rs675504 | 11 | 102959002 | upstream gene variant | A/G | snv | 0.98 | 5 | ||||
rs10919021 | 1 | 162265600 | intron variant | C/T | snv | 0.97 | 1 | ||||
rs2756231 | 10 | 106706654 | intron variant | C/T | snv | 0.98 | 0.97 | 1 | |||
rs453789 | 17 | 44118647 | intron variant | A/C | snv | 0.97 | 1 | ||||
rs567279 | 1 | 66222346 | intron variant | G/T | snv | 0.97 | 4 | ||||
rs11784828 | 8 | 10333788 | intron variant | T/G | snv | 0.97 | 1 | ||||
rs6561821 | 13 | 33287048 | intron variant | A/T | snv | 0.97 | 1 | ||||
rs1337068 | 1 | 162163356 | intron variant | G/A | snv | 0.96 | 1 | ||||
rs1572521 | 1 | 103097312 | intron variant | T/G | snv | 0.96 | 1 | ||||
rs480392 | 1 | 107436774 | synonymous variant | A/C | snv | 0.99 | 0.95 | 3 | |||
rs2581473 | 15 | 99656452 | intron variant | A/G | snv | 0.95 | 1 | ||||
rs222826 | 0.851 | 0.120 | 2 | 146120964 | regulatory region variant | T/C | snv | 0.94 | 16 | ||
rs7190256 | 0.851 | 0.120 | 16 | 72963084 | intron variant | C/T | snv | 0.94 | 16 | ||
rs4233488 | 1 | 41315341 | intron variant | T/C | snv | 0.94 | 1 | ||||
rs2072560 | 11 | 116791110 | missense variant | T/C | snv | 0.89 | 0.94 | 5 | |||
rs6726798 | 2 | 218436132 | intron variant | A/C | snv | 0.94 | 3 | ||||
rs6589565 | 11 | 116769521 | intron variant | A/G | snv | 0.93 | 5 | ||||
rs10790162 | 0.882 | 0.160 | 11 | 116768388 | intron variant | A/G;T | snv | 0.93 | 7 | ||
rs7350481 | 0.882 | 0.040 | 11 | 116715567 | regulatory region variant | T/C | snv | 0.93 | 8 |