Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs505922 | 0.689 | 0.520 | 9 | 133273813 | intron variant | C/T | snv | 34 | |||
rs635634 | 0.882 | 0.160 | 9 | 133279427 | upstream gene variant | T/A;C | snv | 22 | |||
rs651007 | 0.851 | 0.160 | 9 | 133278431 | upstream gene variant | T/A;C | snv | 22 | |||
rs657152 | 0.882 | 0.200 | 9 | 133263862 | intron variant | A/C;T | snv | 22 | |||
rs687621 | 0.851 | 0.240 | 9 | 133261662 | intron variant | G/A;C | snv | 18 | |||
rs2519093 | 0.882 | 0.200 | 9 | 133266456 | intron variant | T/C | snv | 16 | |||
rs687289 | 1.000 | 0.120 | 9 | 133261703 | intron variant | A/G | snv | 15 | |||
rs529565 | 0.851 | 0.120 | 9 | 133274084 | intron variant | C/T | snv | 13 | |||
rs550057 | 0.925 | 0.080 | 9 | 133271182 | intron variant | T/A;C | snv | 11 | |||
rs514659 | 0.882 | 0.120 | 9 | 133266790 | intron variant | C/A;T | snv | 10 | |||
rs6050 | 0.827 | 0.120 | 4 | 154586438 | missense variant | T/A;C | snv | 0.29 | 10 | ||
rs612169 | 9 | 133268030 | intron variant | G/A | snv | 10 | |||||
rs649129 | 1.000 | 0.080 | 9 | 133278860 | upstream gene variant | T/C;G | snv | 10 | |||
rs630014 | 9 | 133274306 | intron variant | G/A;C | snv | 9 | |||||
rs507666 | 1.000 | 0.040 | 9 | 133273983 | intron variant | A/G | snv | 8 | |||
rs545971 | 9 | 133267960 | intron variant | T/A;C | snv | 8 | |||||
rs643434 | 9 | 133266942 | intron variant | A/G;T | snv | 8 | |||||
rs674302 | 9 | 133271249 | intron variant | A/T | snv | 8 | |||||
rs4444878 | 0.851 | 0.120 | 4 | 186292729 | intron variant | C/A;T | snv | 7 | |||
rs644234 | 9 | 133266804 | intron variant | G/T | snv | 7 | |||||
rs1593 | 4 | 186274397 | 3 prime UTR variant | T/A;G | snv | 3 | |||||
rs2073827 | 9 | 133261730 | intron variant | G/C | snv | 3 | |||||
rs4253417 | 4 | 186277851 | intron variant | T/C;G | snv | 3 | |||||
rs492488 | 9 | 133269548 | intron variant | A/C;G;T | snv | 3 | |||||
rs532436 | 1.000 | 0.080 | 9 | 133274414 | intron variant | A/G;T | snv | 3 |