Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs145285408 | 7 | 11345523 | intron variant | G/C | snv | 2.4E-03 | 2 | ||||
rs187281066 | 3 | 132157410 | intron variant | A/G | snv | 1.4E-05 | 2 | ||||
rs112409831 | 3 | 132417596 | 5 prime UTR variant | C/T | snv | 2.3E-02 | 2 | ||||
rs16839481 | 3 | 132660153 | 5 prime UTR variant | G/A | snv | 1.1E-02 | 2 | ||||
rs192622883 | 3 | 133150563 | intron variant | A/G | snv | 2.5E-04 | 2 | ||||
rs183511413 | 3 | 133330418 | intron variant | A/G | snv | 2.3E-04 | 2 | ||||
rs9872999 | 3 | 133738670 | intron variant | C/G;T | snv | 2 | |||||
rs8177248 | 1.000 | 0.040 | 3 | 133760782 | non coding transcript exon variant | C/T | snv | 0.28 | 3 | ||
rs8177253 | 1.000 | 0.040 | 3 | 133761348 | non coding transcript exon variant | C/T | snv | 0.31 | 3 | ||
rs6762719 | 3 | 133761973 | non coding transcript exon variant | A/G | snv | 0.31 | 4 | ||||
rs3811647 | 0.807 | 0.120 | 3 | 133765185 | intron variant | G/A | snv | 0.31 | 15 | ||
rs7637997 | 3 | 133864120 | intron variant | G/A;C;T | snv | 2 | |||||
rs187472012 | 3 | 134820915 | intron variant | A/G | snv | 2.7E-04 | 2 | ||||
rs183252871 | 3 | 134964503 | intron variant | T/C;G | snv | 2 | |||||
rs9824310 | 3 | 159474954 | intron variant | A/G | snv | 0.68 | 2 | ||||
rs78455250 | 1 | 189052039 | intergenic variant | G/A;C | snv | 2 | |||||
rs74138220 | 1 | 189188129 | intergenic variant | G/A | snv | 3.8E-03 | 2 | ||||
rs12052498 | 2 | 189497185 | intergenic variant | G/A | snv | 0.39 | 2 | ||||
rs9813476 | 3 | 197992314 | intron variant | C/T | snv | 3.7E-02 | 2 | ||||
rs183360145 | 6 | 25296893 | intron variant | T/C | snv | 2.6E-03 | 2 | ||||
rs116009877 | 6 | 25715429 | regulatory region variant | G/A;T | snv | 4 | |||||
rs80215559 | 6 | 25917997 | intron variant | T/C | snv | 3.7E-02 | 3 | ||||
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 262 | |
rs78545713 | 6 | 26248612 | upstream gene variant | A/G;T | snv | 2 | |||||
rs13191659 | 6 | 27033276 | intron variant | C/G;T | snv | 4 |