Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10456943 | 6 | 121556819 | regulatory region variant | A/C | snv | 0.11 | 1 | ||||
rs10460436 | 2 | 231950631 | intergenic variant | G/A | snv | 5.7E-02 | 1 | ||||
rs10463076 | 5 | 160177301 | intergenic variant | G/A | snv | 0.16 | 1 | ||||
rs10472828 | 5 | 32888712 | non coding transcript exon variant | C/T | snv | 0.40 | 1 | ||||
rs10479944 | 7 | 15074211 | intergenic variant | T/A | snv | 0.13 | 1 | ||||
rs10514714 | 3 | 46594334 | intron variant | G/T | snv | 5.9E-02 | 1 | ||||
rs10516446 | 4 | 99629967 | upstream gene variant | T/A | snv | 0.19 | 1 | ||||
rs10517245 | 4 | 52163519 | intergenic variant | G/A | snv | 0.15 | 1 | ||||
rs10519170 | 15 | 48393978 | regulatory region variant | A/G | snv | 0.18 | 1 | ||||
rs1052483 | 2 | 219069626 | non coding transcript exon variant | G/T | snv | 0.13 | 1 | ||||
rs10526240 | 11 | 58004066 | upstream gene variant | T/A;G | snv | 1 | |||||
rs10746837 | 9 | 88258738 | regulatory region variant | G/A | snv | 0.49 | 1 | ||||
rs10747784 | 12 | 57857579 | intergenic variant | G/A;C;T | snv | 1 | |||||
rs10748128 | 12 | 69433878 | intergenic variant | G/T | snv | 0.42 | 1 | ||||
rs10756851 | 9 | 16991334 | intron variant | G/A | snv | 0.50 | 1 | ||||
rs10773100 | 12 | 124695033 | TF binding site variant | C/G;T | snv | 1 | |||||
rs10779122 | 12 | 84661783 | regulatory region variant | T/C | snv | 0.36 | 1 | ||||
rs10781573 | 10 | 132420104 | intron variant | C/A;T | snv | 0.69 | 1 | ||||
rs10784445 | 12 | 65272610 | intergenic variant | A/G;T | snv | 1 | |||||
rs10795075 | 10 | 3773988 | downstream gene variant | C/T | snv | 0.35 | 1 | ||||
rs10798580 | 1 | 177895419 | intron variant | G/A | snv | 0.36 | 1 | ||||
rs10799445 | 1 | 227724182 | upstream gene variant | A/C | snv | 0.27 | 1 | ||||
rs10811888 | 9 | 23325086 | intron variant | T/C | snv | 0.52 | 1 | ||||
rs10826579 | 10 | 29202607 | regulatory region variant | G/A;T | snv | 1 | |||||
rs10847415 | 12 | 122659746 | regulatory region variant | T/A;C | snv | 1 |