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 | ||||
rs2194411 | 3 | 185830875 | intergenic variant | G/A;C | snv | 2 | |||||
rs28778940 | 9 | 95536070 | intergenic variant | G/A | snv | 0.31 | 2 | ||||
rs2900208 | 12 | 11725530 | intron variant | C/A | snv | 0.29 | 2 | ||||
rs35320790 | 14 | 60642107 | intron variant | C/A;G | snv | 2 | |||||
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 | ||||
rs4373984 | 12 | 97398809 | intergenic variant | C/T | snv | 0.55 | 2 | ||||
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 | ||||
rs59985551 | 2 | 55879793 | intron variant | C/T | snv | 0.21 | 2 | ||||
rs62372052 | 5 | 42724192 | upstream gene variant | A/G | snv | 6.9E-02 | 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 | ||||
rs6899155 | 5 | 36786357 | intergenic variant | T/C | snv | 0.44 | 2 | ||||
rs74494415 | 18 | 77260182 | intron variant | C/A;T | snv | 2 | |||||
rs76307059 | 6 | 168600208 | intron variant | C/A;G;T | snv | 2 | |||||
rs147110934 | 19 | 55482069 | missense variant | G/T | snv | 1.4E-02 | 1.5E-02 | 3 | |||
rs16942341 | 15 | 88845674 | synonymous variant | C/T | snv | 3.8E-02 | 6.4E-02 | 3 | |||
rs35506085 | 11 | 2144346 | intron variant | G/A | snv | 0.17 | 3 |