Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4444235 | 0.701 | 0.240 | 14 | 53944201 | downstream gene variant | T/C | snv | 0.43 | 23 | ||
rs12229654 | 0.763 | 0.320 | 12 | 110976657 | intergenic variant | T/G | snv | 4.8E-03 | 20 | ||
rs1321311 | 0.742 | 0.160 | 6 | 36655123 | regulatory region variant | C/A | snv | 0.28 | 15 | ||
rs10484761 | 0.807 | 0.080 | 6 | 40834522 | intergenic variant | T/C | snv | 0.31 | 7 | ||
rs12413624 | 0.851 | 0.120 | 10 | 118519432 | intergenic variant | T/A | snv | 0.34 | 5 | ||
rs31563 | 0.851 | 0.160 | 5 | 135899917 | intron variant | C/A;T | snv | 5 | |||
rs312986 | 0.925 | 0.080 | 18 | 1898710 | intron variant | A/G;T | snv | 3 | |||
rs1430055 | 2 | 16499521 | intergenic variant | G/A | snv | 0.61 | 2 | ||||
rs6503659 | 1.000 | 0.040 | 17 | 41741012 | intergenic variant | A/C;G;T | snv | 2 | |||
rs6772209 | 1.000 | 0.080 | 3 | 175929377 | intergenic variant | G/A | snv | 4.1E-02 | 2 | ||
rs7578456 | 1.000 | 0.080 | 2 | 201370625 | intergenic variant | A/G | snv | 0.57 | 2 | ||
rs8030672 | 1.000 | 0.080 | 15 | 68766745 | intergenic variant | T/A | snv | 5.4E-02 | 2 | ||
rs10502995 | 18 | 55138645 | regulatory region variant | G/A | snv | 0.20 | 1 | ||||
rs11972901 | 7 | 85966605 | intergenic variant | A/G | snv | 0.47 | 1 | ||||
rs1453029 | 18 | 41000207 | intergenic variant | T/C | snv | 7.0E-02 | 1 | ||||
rs1737076 | 6 | 29757544 | intron variant | A/G | snv | 0.45 | 1 | ||||
rs17450420 | 13 | 104386796 | intergenic variant | A/G | snv | 5.9E-02 | 1 | ||||
rs2378002 | 1 | 218749016 | intergenic variant | G/T | snv | 5.9E-02 | 1 | ||||
rs2984526 | 9 | 72372344 | intergenic variant | C/G | snv | 0.48 | 1 | ||||
rs4283388 | 2 | 172374994 | downstream gene variant | C/T | snv | 0.33 | 1 | ||||
rs4503732 | 15 | 46350065 | intron variant | C/A;G;T | snv | 0.92 | 1 | ||||
rs6023640 | 20 | 54842266 | intergenic variant | T/G | snv | 0.73 | 1 | ||||
rs7206735 | 16 | 50114597 | intron variant | T/C | snv | 0.39 | 1 | ||||
rs753544 | 6 | 29812752 | upstream gene variant | C/T | snv | 0.27 | 1 | ||||
rs896570 | 10 | 47145727 | intergenic variant | C/T | snv | 0.50 | 1 |