Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10049413 | 3 | 49855463 | intron variant | A/G | snv | 0.24 | 1 | ||||
rs1007934 | 14 | 72996771 | intron variant | G/A | snv | 0.33 | 3 | ||||
rs1008084 | 6 | 109305762 | intron variant | G/A | snv | 0.40 | 1 | ||||
rs1009110 | 17 | 73199810 | intron variant | C/T | snv | 0.52 | 1 | ||||
rs10092747 | 8 | 119736926 | intron variant | C/G;T | snv | 1 | |||||
rs10107630 | 8 | 129591389 | intron variant | C/T | snv | 0.54 | 3 | ||||
rs1011167 | 7 | 21489977 | intron variant | A/C | snv | 0.33 | 1 | ||||
rs10137527 | 14 | 105134327 | intron variant | C/T | snv | 8.3E-02 | 1 | ||||
rs10159477 | 10 | 69340132 | intron variant | G/A | snv | 0.14 | 1 | ||||
rs10160596 | 11 | 65583893 | non coding transcript exon variant | G/A | snv | 0.20 | 3 | ||||
rs10164806 | 2 | 144435759 | intron variant | C/T | snv | 6.7E-02 | 2 | ||||
rs10165255 | 2 | 10059474 | intron variant | A/G | snv | 0.59 | 2 | ||||
rs10168349 | 2 | 46133768 | intron variant | G/C | snv | 0.36 | 3 | ||||
rs10191559 | 2 | 181075915 | intron variant | G/A | snv | 0.76 | 1 | ||||
rs10197140 | 2 | 110852366 | intron variant | T/C | snv | 0.28 | 3 | ||||
rs10205410 | 2 | 54572462 | intron variant | G/T | snv | 0.31 | 1 | ||||
rs1021797 | 12 | 26413499 | intron variant | A/C | snv | 4.7E-02 | 1 | ||||
rs10224210 | 1.000 | 0.040 | 7 | 151716108 | intron variant | T/C | snv | 0.21 | 8 | ||
rs10226458 | 7 | 47595969 | intergenic variant | T/A | snv | 0.65 | 1 | ||||
rs102275 | 0.827 | 0.320 | 11 | 61790331 | non coding transcript exon variant | T/C | snv | 0.47 | 10 | ||
rs10305916 | 4 | 147536174 | intron variant | T/G | snv | 0.21 | 1 | ||||
rs1037116 | 15 | 101528701 | upstream gene variant | C/T | snv | 0.20 | 2 | ||||
rs10415135 | 19 | 4061546 | intron variant | C/T | snv | 0.23 | 3 | ||||
rs10421876 | 19 | 32871878 | upstream gene variant | C/T | snv | 0.36 | 1 | ||||
rs10423902 | 19 | 33273956 | intergenic variant | G/A;T | snv | 1 |