Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs579459 | 0.752 | 0.320 | 9 | 133278724 | upstream gene variant | C/T | snv | 0.81 | 17 | ||
rs657152 | 0.882 | 0.200 | 9 | 133263862 | intron variant | A/C;T | snv | 14 | |||
rs505922 | 0.689 | 0.520 | 9 | 133273813 | intron variant | C/T | snv | 12 | |||
rs651007 | 0.851 | 0.160 | 9 | 133278431 | upstream gene variant | T/A;C | snv | 11 | |||
rs612169 | 9 | 133268030 | intron variant | G/A | snv | 10 | |||||
rs630014 | 9 | 133274306 | intron variant | G/A;C | snv | 9 | |||||
rs687289 | 1.000 | 0.120 | 9 | 133261703 | intron variant | A/G | snv | 9 | |||
rs687621 | 0.851 | 0.240 | 9 | 133261662 | intron variant | G/A;C | snv | 9 | |||
rs495828 | 0.827 | 0.200 | 9 | 133279294 | upstream gene variant | T/G | snv | 0.81 | 8 | ||
rs514659 | 0.882 | 0.120 | 9 | 133266790 | intron variant | C/A;T | snv | 8 | |||
rs529565 | 0.851 | 0.120 | 9 | 133274084 | intron variant | C/T | snv | 8 | |||
rs545971 | 9 | 133267960 | intron variant | T/A;C | snv | 8 | |||||
rs649129 | 1.000 | 0.080 | 9 | 133278860 | upstream gene variant | T/C;G | snv | 8 | |||
rs674302 | 9 | 133271249 | intron variant | A/T | snv | 8 | |||||
rs635634 | 0.882 | 0.160 | 9 | 133279427 | upstream gene variant | T/A;C | snv | 7 | |||
rs643434 | 9 | 133266942 | intron variant | A/G;T | snv | 7 | |||||
rs644234 | 9 | 133266804 | intron variant | G/T | snv | 7 | |||||
rs2066861 | 4 | 154606284 | intron variant | C/T | snv | 0.26 | 5 | ||||
rs6050 | 0.827 | 0.120 | 4 | 154586438 | missense variant | T/A;C | snv | 0.29 | 5 | ||
rs7681423 | 4 | 154621096 | intergenic variant | C/T | snv | 0.26 | 5 | ||||
rs2420371 | 1 | 169522317 | intron variant | G/A | snv | 0.95 | 4 | ||||
rs3758348 | 9 | 133372523 | intron variant | G/C | snv | 0.13 | 4 | ||||
rs514708 | 9 | 133258352 | intron variant | C/T | snv | 0.29 | 4 | ||||
rs626035 | 9 | 133259603 | intron variant | T/G | snv | 0.28 | 4 | ||||
rs641943 | 9 | 133258323 | intron variant | A/G | snv | 0.29 | 4 |