Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs972982 | 6 | 142345724 | intron variant | T/C | snv | 0.44 | 2 | ||||
rs10037512 | 5 | 89058858 | intron variant | T/A;C | snv | 1 | |||||
rs10058074 | 5 | 132350453 | intron variant | G/A | snv | 0.31 | 1 | ||||
rs1013209 | 8 | 24258791 | intergenic variant | C/T | snv | 0.28 | 1 | ||||
rs10152591 | 15 | 69755818 | intron variant | A/C | snv | 9.8E-02 | 1 | ||||
rs10187066 | 2 | 218650036 | intron variant | A/G | snv | 0.45 | 1 | ||||
rs10231759 | 7 | 150815084 | regulatory region variant | T/C | snv | 0.41 | 1 | ||||
rs1029534 | 7 | 28149464 | intron variant | T/C;G | snv | 1 | |||||
rs10401193 | 19 | 19480257 | intron variant | A/G | snv | 0.19 | 1 | ||||
rs1043515 | 17 | 38765943 | 3 prime UTR variant | A/G | snv | 0.46 | 1 | ||||
rs1047014 | 6 | 19841262 | 3 prime UTR variant | T/C | snv | 0.23 | 1 | ||||
rs10472828 | 5 | 32888712 | non coding transcript exon variant | C/T | snv | 0.40 | 1 | ||||
rs10492321 | 12 | 93586312 | downstream gene variant | T/A | snv | 0.20 | 1 | ||||
rs10513137 | 3 | 141424588 | intron variant | G/A;C | snv | 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 | ||||
rs1074683 | 20 | 33716847 | intron variant | C/G | snv | 0.24 | 1 | ||||
rs10748128 | 12 | 69433878 | intergenic variant | G/T | snv | 0.42 | 1 | ||||
rs10770705 | 12 | 20704533 | intron variant | A/C | snv | 0.70 | 1 | ||||
rs10799445 | 1 | 227724182 | upstream gene variant | A/C | snv | 0.27 | 1 | ||||
rs10838708 | 11 | 47419962 | intron variant | G/A | snv | 0.39 | 1 | ||||
rs10838798 | 11 | 48069751 | intron variant | T/G | snv | 0.56 | 1 | ||||
rs10838801 | 11 | 48076728 | intron variant | G/A | snv | 0.56 | 1 | ||||
rs10843164 | 12 | 28416781 | intron variant | T/C | snv | 0.22 | 1 | ||||
rs10859563 | 12 | 93726563 | intron variant | C/G | snv | 0.40 | 1 |