Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10416839 | 1.000 | 0.040 | 19 | 41776424 | intron variant | G/T | snv | 0.26 | 1 | ||
rs11133504 | 1.000 | 0.040 | 4 | 57514156 | intergenic variant | G/A | snv | 0.23 | 1 | ||
rs11739663 | 1.000 | 0.040 | 5 | 593968 | intergenic variant | T/C | snv | 0.29 | 1 | ||
rs13337840 | 1.000 | 0.040 | 16 | 86793733 | intergenic variant | A/G | snv | 0.28 | 1 | ||
rs16940186 | 1.000 | 0.040 | 16 | 85976134 | intron variant | T/C | snv | 0.17 | 1 | ||
rs17771967 | 1.000 | 0.040 | 19 | 54868759 | downstream gene variant | A/G | snv | 0.42 | 1 | ||
rs1830610 | 1.000 | 0.040 | 9 | 5260079 | intergenic variant | C/G;T | snv | 1 | |||
rs2457996 | 1.000 | 0.040 | 4 | 73990818 | upstream gene variant | C/A;G;T | snv | 1 | |||
rs2764742 | 1.000 | 0.040 | 16 | 20019510 | intergenic variant | C/A;T | snv | 1 | |||
rs4510766 | 1.000 | 0.040 | 7 | 107852344 | intergenic variant | A/G | snv | 0.36 | 1 | ||
rs4722672 | 1.000 | 0.040 | 7 | 27192143 | intron variant | C/T | snv | 0.73 | 1 | ||
rs6437358 | 1.000 | 0.040 | 2 | 240657733 | intergenic variant | G/C | snv | 0.33 | 1 | ||
rs6451493 | 1.000 | 0.040 | 5 | 40410833 | upstream gene variant | G/A;T | snv | 1 | |||
rs6951457 | 1.000 | 0.040 | 7 | 107815875 | intergenic variant | G/A;C | snv | 1 | |||
rs7911117 | 1.000 | 0.040 | 10 | 26890667 | regulatory region variant | T/G | snv | 0.18 | 1 | ||
rs886774 | 1.000 | 0.040 | 7 | 107854989 | regulatory region variant | G/A | snv | 0.67 | 1 | ||
rs9271209 | 1.000 | 0.040 | 6 | 32611258 | intergenic variant | G/A | snv | 0.74 | 1 | ||
rs943072 | 1.000 | 0.040 | 6 | 43828231 | intron variant | G/T | snv | 0.83 | 1 | ||
rs9548988 | 1.000 | 0.040 | 13 | 39931373 | regulatory region variant | C/T | snv | 0.44 | 1 | ||
rs3740415 | 1.000 | 0.040 | 10 | 102472959 | 3 prime UTR variant | G/A | snv | 0.48 | 0.48 | 1 | |
rs4725479 | 1.000 | 0.040 | 7 | 153048725 | intergenic variant | T/C | snv | 0.64 | 1 | ||
rs2241877 | 1.000 | 0.040 | 2 | 233277843 | intron variant | A/G | snv | 0.69 | 1 | ||
rs6911490 | 1.000 | 0.040 | 6 | 106074152 | intron variant | T/C | snv | 0.86 | 1 | ||
rs41417449 | 1.000 | 0.040 | 6 | 32396234 | missense variant | T/C | snv | 2.3E-02 | 9.5E-03 | 1 | |
rs254562 | 1.000 | 0.040 | 5 | 135105767 | intron variant | A/G | snv | 0.32 | 1 |