Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7310615 | 0.882 | 12 | 111427245 | intron variant | C/G | snv | 0.67 | 12 | |||
rs11086102 | 0.882 | 19 | 18287818 | upstream gene variant | G/C | snv | 0.64 | 6 | |||
rs2075302 | 0.882 | 2 | 162219636 | intron variant | T/C | snv | 0.34 | 5 | |||
rs5754100 | 0.882 | 22 | 21561877 | intron variant | T/C | snv | 0.18 | 5 | |||
rs73316435 | 0.882 | 17 | 47252111 | upstream gene variant | C/A;T | snv | 5 | ||||
rs10202630 | 0.882 | 2 | 190398199 | intergenic variant | T/C | snv | 0.52 | 4 | |||
rs10444776 | 0.882 | 14 | 105647030 | upstream gene variant | G/A;T | snv | 4 | ||||
rs10494079 | 0.882 | 1 | 107832253 | intron variant | G/C | snv | 9.0E-02 | 4 | |||
rs10937560 | 0.882 | 3 | 192909627 | intron variant | G/C | snv | 0.45 | 4 | |||
rs10986284 | 0.882 | 9 | 124236874 | intergenic variant | A/T | snv | 0.27 | 4 | |||
rs11746555 | 0.882 | 5 | 132391341 | intron variant | G/A | snv | 0.28 | 4 | |||
rs11785816 | 0.882 | 8 | 128518940 | intron variant | C/A;G | snv | 4 | ||||
rs1199047 | 0.882 | 11 | 64350711 | intron variant | A/C | snv | 0.38 | 4 | |||
rs12980063 | 0.882 | 19 | 49693735 | intron variant | A/G | snv | 0.48 | 4 | |||
rs1320344 | 0.882 | 12 | 103493699 | intron variant | A/G | snv | 0.64 | 4 | |||
rs13299616 | 0.882 | 9 | 120832525 | intron variant | T/C | snv | 0.50 | 4 | |||
rs13380830 | 0.882 | 17 | 42145640 | intron variant | C/G | snv | 0.29 | 4 | |||
rs142647938 | 0.882 | 2 | 162516642 | intron variant | C/A;T | snv | 4 | ||||
rs145268310 | 0.882 | 3 | 12269274 | regulatory region variant | G/C | snv | 9.9E-02 | 4 | |||
rs1530687 | 0.882 | 3 | 119395668 | intron variant | G/A | snv | 0.46 | 4 | |||
rs1549922 | 0.882 | 5 | 159304540 | intergenic variant | G/A | snv | 0.56 | 4 | |||
rs1790588 | 0.882 | 18 | 69867948 | intron variant | T/C | snv | 0.55 | 4 | |||
rs1800601 | 0.882 | 1 | 156815825 | 5 prime UTR variant | G/A;T | snv | 0.67; 4.0E-06 | 4 | |||
rs191252491 | 0.882 | 12 | 111773070 | intron variant | A/T | snv | 7.1E-03 | 4 | |||
rs1921445 | 0.882 | 3 | 106229671 | intergenic variant | A/C;G | snv | 4 |