Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs35883536 | 1 | 100640978 | non coding transcript exon variant | G/A | snv | 0.46 | 2 | ||||
rs4807440 | 19 | 1026478 | upstream gene variant | G/T | snv | 0.65 | 3 | ||||
rs562752749 | 10 | 102805443 | intron variant | TT/-;T;TTT;TTTT;TTTTT;TTTTTTT;TTTTTTTTTTTT | delins | 2 | |||||
rs12898000 | 14 | 103368791 | upstream gene variant | G/C;T | snv | 2 | |||||
rs8022179 | 14 | 103380950 | upstream gene variant | T/A;C | snv | 2 | |||||
rs7298732 | 12 | 10458392 | upstream gene variant | T/C | snv | 9.8E-02 | 2 | ||||
rs199741557 | 4 | 104943373 | intron variant | TC/- | delins | 2.6E-02 | 2 | ||||
rs605783 | 6 | 10526140 | intron variant | T/A | snv | 0.65 | 2 | ||||
rs9480737 | 6 | 107121073 | intergenic variant | A/G | snv | 0.33 | 2 | ||||
rs12312487 | 12 | 108327859 | intron variant | G/A | snv | 0.31 | 2 | ||||
rs150861794 | 13 | 108351457 | intron variant | C/T | snv | 1.7E-02 | 2 | ||||
rs75900305 | 13 | 109159737 | intron variant | -/C | delins | 0.25 | 2 | ||||
rs1887639 | 13 | 109374581 | intergenic variant | T/C | snv | 0.42 | 2 | ||||
rs17608459 | 1 | 109892706 | upstream gene variant | G/A | snv | 7.9E-02 | 2 | ||||
rs333947 | 1 | 109928142 | intron variant | G/A | snv | 0.13 | 7 | ||||
rs58814158 | 13 | 110167908 | intron variant | T/G | snv | 0.12 | 2 | ||||
rs2062225 | 2 | 110993295 | intron variant | A/C;T | snv | 2 | |||||
rs150449635 | 2 | 110994574 | intron variant | T/C | snv | 1.5E-02 | 2 | ||||
rs3789088 | 2 | 111033227 | intron variant | G/C | snv | 0.14 | 2 | ||||
rs3789087 | 2 | 111034076 | intron variant | C/T | snv | 0.14 | 2 | ||||
rs7578982 | 2 | 111078961 | intron variant | T/C | snv | 0.27 | 2 | ||||
rs10980797 | 9 | 111150273 | intron variant | A/G;T | snv | 3 | |||||
rs6734942 | 2 | 111153117 | intron variant | C/G;T | snv | 2 | |||||
rs10980800 | 9 | 111153625 | intron variant | T/C | snv | 0.21 | 2 | ||||
rs12346772 | 9 | 111158319 | intron variant | A/G | snv | 0.18 | 2 |