Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1007934 | 14 | 72996771 | intron variant | G/A | snv | 0.33 | 3 | ||||
rs1008084 | 6 | 109305762 | intron variant | G/A | snv | 0.40 | 3 | ||||
rs1010222 | 19 | 12937794 | upstream gene variant | A/G | snv | 0.70 | 3 | ||||
rs10107630 | 8 | 129591389 | intron variant | C/T | snv | 0.54 | 3 | ||||
rs10160596 | 11 | 65583893 | non coding transcript exon variant | G/A | snv | 0.20 | 3 | ||||
rs10197140 | 2 | 110852366 | intron variant | T/C | snv | 0.28 | 3 | ||||
rs10415135 | 19 | 4061546 | intron variant | C/T | snv | 0.23 | 3 | ||||
rs1050828 | 0.790 | 0.200 | X | 154536002 | missense variant | C/T | snv | 9.1E-03 | 3.6E-02 | 15 | |
rs10758656 | 9 | 4852599 | intron variant | A/G | snv | 0.19 | 7 | ||||
rs10758658 | 9 | 4856877 | intron variant | G/A | snv | 0.15 | 4 | ||||
rs10766533 | 11 | 19203130 | intron variant | T/A | snv | 0.62 | 4 | ||||
rs10772280 | 12 | 10428441 | intron variant | C/A;T | snv | 2 | |||||
rs10793565 | 10 | 44892783 | intron variant | G/C | snv | 0.53 | 3 | ||||
rs10849020 | 12 | 4222843 | intergenic variant | C/G | snv | 0.22 | 3 | ||||
rs10849023 | 12 | 4223312 | intergenic variant | C/T | snv | 0.22 | 4 | ||||
rs10910476 | 1 | 234599210 | regulatory region variant | C/A;T | snv | 2 | |||||
rs10974716 | 9 | 4661574 | intron variant | C/G | snv | 0.20 | 2 | ||||
rs11085824 | 19 | 12890733 | upstream gene variant | A/G | snv | 0.31 | 4 | ||||
rs11085825 | 19 | 12896644 | intron variant | C/T | snv | 0.31 | 3 | ||||
rs11158716 | 14 | 68026441 | intron variant | G/A | snv | 0.17 | 2 | ||||
rs11211480 | 1 | 47227548 | non coding transcript exon variant | A/G | snv | 0.42 | 4 | ||||
rs112233623 | 6 | 41957260 | intron variant | C/T | snv | 7.0E-03 | 5 | ||||
rs112257498 | 2 | 189568259 | intron variant | C/G;T | snv | 2 | |||||
rs11244669 | 10 | 125844213 | intron variant | A/C | snv | 0.28 | 4 | ||||
rs113809617 | 9 | 137205865 | missense variant | C/G | snv | 0.13 | 0.12 | 5 |