Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 30 | |
rs11014285 | 10 | 24889935 | intron variant | G/A | snv | 0.11 | 2 | ||||
rs12509014 | 4 | 122904764 | intron variant | C/T | snv | 0.63 | 2 | ||||
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 64 | |
rs143384 | 0.827 | 0.200 | 20 | 35437976 | 5 prime UTR variant | G/A | snv | 0.44 | 14 | ||
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 | |||
rs212526 | 1 | 21258448 | intron variant | T/C | snv | 0.68 | 2 | ||||
rs2194411 | 3 | 185830875 | intergenic variant | G/A;C | snv | 2 | |||||
rs2277339 | 12 | 56752285 | missense variant | T/G | snv | 0.12 | 0.14 | 10 | |||
rs2812208 | 13 | 50132951 | intron variant | G/A;C | snv | 5 | |||||
rs28778940 | 9 | 95536070 | intergenic variant | G/A | snv | 0.31 | 2 | ||||
rs28929474 | 0.708 | 0.320 | 14 | 94378610 | missense variant | C/G;T | snv | 2.8E-05; 1.1E-02 | 23 | ||
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 | ||||
rs3814333 | 1 | 184037985 | upstream gene variant | C/T | snv | 0.29 | 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 | |||||
rs4373984 | 12 | 97398809 | intergenic variant | C/T | snv | 0.55 | 2 | ||||
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 |