Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11014285 | 10 | 24889935 | intron variant | G/A | snv | 0.11 | 2 | ||||
rs12509014 | 4 | 122904764 | intron variant | C/T | snv | 0.63 | 2 | ||||
rs212526 | 1 | 21258448 | intron variant | T/C | snv | 0.68 | 2 | ||||
rs2812208 | 13 | 50132951 | intron variant | G/A;C | snv | 5 | |||||
rs2900208 | 12 | 11725530 | intron variant | C/A | snv | 0.29 | 2 | ||||
rs34517439 | 0.882 | 0.120 | 1 | 77984833 | intron variant | C/A | snv | 7.3E-02 | 7 | ||
rs35320790 | 14 | 60642107 | intron variant | C/A;G | snv | 2 | |||||
rs35506085 | 11 | 2144346 | intron variant | G/A | snv | 0.17 | 3 | ||||
rs3818416 | 1.000 | 0.080 | 13 | 77900333 | intron variant | A/C | snv | 0.75 | 2 | ||
rs4073717 | 5 | 171437017 | intron variant | G/T | snv | 0.23 | 2 | ||||
rs41271299 | 6 | 19839184 | intron variant | C/A;G;T | snv | 3 | |||||
rs4800148 | 18 | 23144364 | intron variant | G/A;C | snv | 4 | |||||
rs4870941 | 8 | 125486586 | intron variant | G/C | snv | 0.20 | 4 | ||||
rs508347 | 7 | 28173205 | intron variant | T/C | snv | 0.69 | 2 | ||||
rs509035 | 3 | 172445659 | intron variant | G/A | snv | 0.25 | 2 | ||||
rs55745410 | 1 | 33337216 | intron variant | A/G | snv | 0.28 | 2 | ||||
rs5750823 | 22 | 39433968 | intron variant | C/T | snv | 0.70 | 3 | ||||
rs59985551 | 2 | 55879793 | intron variant | C/T | snv | 0.21 | 2 | ||||
rs6711710 | 2 | 223091692 | intron variant | T/C | snv | 0.77 | 2 | ||||
rs6762578 | 3 | 129273204 | intron variant | G/A;T | snv | 2 | |||||
rs6762851 | 3 | 56652301 | intron variant | T/C | snv | 0.50 | 2 | ||||
rs6824748 | 4 | 17995443 | intron variant | G/A | snv | 0.25 | 2 | ||||
rs7223535 | 1.000 | 0.080 | 17 | 30884649 | intron variant | G/A | snv | 0.25 | 4 | ||
rs72656010 | 8 | 56209656 | intron variant | T/C | snv | 0.10 | 3 | ||||
rs74494415 | 18 | 77260182 | intron variant | C/A;T | snv | 2 |