Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7394579 | 1.000 | 0.080 | 11 | 61813978 | intron variant | A/G | snv | 0.22 | 5 | ||
rs11627485 | 14 | 65020976 | intron variant | T/C | snv | 0.36 | 5 | ||||
rs1434282 | 1 | 199041592 | non coding transcript exon variant | C/T | snv | 0.76 | 5 | ||||
rs1569419 | 1 | 3080038 | intron variant | T/C | snv | 0.73 | 5 | ||||
rs78909033 | 2 | 240571486 | intron variant | G/A | snv | 9.2E-02 | 5 | ||||
rs13412535 | 2 | 224010157 | intron variant | G/A | snv | 0.17 | 5 | ||||
rs34651 | 1.000 | 0.040 | 5 | 72848178 | non coding transcript exon variant | C/T | snv | 0.94 | 5 | ||
rs9494145 | 0.925 | 0.080 | 6 | 135111414 | intergenic variant | T/A;C | snv | 4 | |||
rs74847330 | 2 | 143074030 | intergenic variant | A/G | snv | 8.8E-02 | 4 | ||||
rs1354034 | 3 | 56815721 | intron variant | T/C | snv | 0.49 | 4 | ||||
rs56043070 | 1 | 247556467 | splice donor variant | G/A;T | snv | 5.2E-02; 4.1E-06 | 4 | ||||
rs7896518 | 10 | 63344740 | intron variant | A/G | snv | 0.38 | 4 | ||||
rs114694170 | 1.000 | 0.040 | 5 | 88884379 | non coding transcript exon variant | T/C | snv | 3.6E-02 | 4 | ||
rs11734132 | 4 | 6889792 | intergenic variant | G/C | snv | 0.17 | 3 | ||||
rs117672662 | 14 | 68958750 | intron variant | T/C | snv | 7.4E-03 | 3 | ||||
rs17572109 | 2 | 218229211 | non coding transcript exon variant | G/A;T | snv | 3 | |||||
rs3842397 | 18 | 46265918 | 3 prime UTR variant | TT/- | del | 0.43 | 3 | ||||
rs553749201 | 17 | 4933900 | synonymous variant | C/A | snv | 3 | |||||
rs342293 | 0.882 | 0.040 | 7 | 106731773 | intron variant | C/G | snv | 0.42 | 3 | ||
rs139141690 | 7 | 101856650 | intron variant | G/A | snv | 2.2E-03 | 3 | ||||
rs655029 | 2 | 31254972 | intron variant | G/A | snv | 0.78 | 3 | ||||
rs944002 | 14 | 103106478 | intron variant | A/G | snv | 0.25 | 3 | ||||
rs41315846 | 1 | 247549001 | intron variant | T/C | snv | 0.44 | 0.52 | 3 | |||
rs10886430 | 10 | 119250744 | intron variant | A/G | snv | 8.8E-02 | 3 | ||||
rs4907622 | 13 | 113362571 | intron variant | G/C;T | snv | 3 |