Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12743824 | 0.925 | 0.040 | 1 | 99317401 | intergenic variant | C/A | snv | 0.48 | 2 | ||
rs2073080 | 0.925 | 0.040 | 22 | 43998522 | intron variant | C/T | snv | 0.20 | 2 | ||
rs6006473 | 0.925 | 0.040 | 22 | 43997195 | intron variant | C/T | snv | 0.47 | 2 | ||
rs1977081 | 1.000 | 22 | 43934248 | intron variant | T/C;G | snv | 2 | ||||
rs3761472 | 0.925 | 0.040 | 22 | 43972242 | missense variant | A/G | snv | 0.21 | 0.18 | 2 | |
rs4823182 | 0.925 | 0.080 | 22 | 43981562 | intron variant | A/G | snv | 0.46 | 2 | ||
rs72563732 | 0.882 | 0.040 | 3 | 186854563 | synonymous variant | C/T | snv | 6.4E-05 | 2.6E-04 | 3 | |
rs12447924 | 1.000 | 16 | 56960280 | upstream gene variant | C/T | snv | 0.76 | 3 | |||
rs12597002 | 1.000 | 16 | 56968492 | intron variant | C/A | snv | 0.25 | 3 | |||
rs7643645 | 0.882 | 0.080 | 3 | 119806650 | intron variant | A/G | snv | 0.31 | 3 | ||
rs2072907 | 0.882 | 0.120 | 22 | 43936773 | intron variant | C/G | snv | 0.20 | 3 | ||
rs2076211 | 1.000 | 22 | 43933198 | intron variant | C/A;T | snv | 0.18 | 3 | |||
rs2290602 | 0.882 | 0.040 | 4 | 23824109 | intron variant | T/A;G | snv | 3 | |||
rs2235776 | 0.925 | 0.040 | 22 | 43982119 | intron variant | C/T | snv | 0.24 | 3 | ||
rs738491 | 0.882 | 0.040 | 22 | 43958231 | intron variant | C/T | snv | 0.34 | 3 | ||
rs903361 | 0.882 | 0.160 | 1 | 203122146 | intron variant | G/A;C | snv | 4 | |||
rs1010023 | 0.851 | 0.080 | 22 | 43940218 | intron variant | T/C | snv | 0.20 | 4 | ||
rs12483959 | 1.000 | 22 | 43930116 | intron variant | G/A;C;T | snv | 4 | ||||
rs2072906 | 0.851 | 0.160 | 22 | 43937292 | intron variant | A/G | snv | 0.25 | 0.20 | 4 | |
rs951599607 | 0.925 | 0.040 | 3 | 12434028 | missense variant | G/A | snv | 4 | |||
rs2645424 | 0.827 | 0.120 | 8 | 11826954 | intron variant | A/C;G | snv | 0.56 | 5 | ||
rs1461729 | 1.000 | 8 | 9329732 | intron variant | A/G | snv | 0.88 | 5 | |||
rs6601299 | 0.925 | 0.040 | 8 | 9327181 | intron variant | T/C | snv | 0.88 | 5 | ||
rs2143571 | 0.827 | 0.080 | 22 | 43995806 | intron variant | G/A | snv | 0.25 | 5 | ||
rs2071303 | 0.882 | 0.120 | 6 | 26091108 | splice region variant | T/C | snv | 0.38 | 0.36 | 6 |