Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1572982 | 0.827 | 0.200 | 6 | 26094139 | intron variant | G/A;T | snv | 0.52; 8.0E-06 | 7 | ||
rs2143571 | 0.827 | 0.080 | 22 | 43995806 | intron variant | G/A | snv | 0.25 | 5 | ||
rs2645424 | 0.827 | 0.120 | 8 | 11826954 | intron variant | A/C;G | snv | 0.56 | 5 | ||
rs2281135 | 0.851 | 0.160 | 22 | 43936690 | intron variant | G/A | snv | 0.19 | 10 | ||
rs9940128 | 0.851 | 0.120 | 16 | 53766842 | intron variant | G/A | snv | 0.42 | 10 | ||
rs7946 | 0.851 | 0.160 | 17 | 17506246 | missense variant | C/T | snv | 0.59 | 0.59 | 6 | |
rs1010023 | 0.851 | 0.080 | 22 | 43940218 | intron variant | T/C | snv | 0.20 | 4 | ||
rs2072906 | 0.851 | 0.160 | 22 | 43937292 | intron variant | A/G | snv | 0.25 | 0.20 | 4 | |
rs2071303 | 0.882 | 0.120 | 6 | 26091108 | splice region variant | T/C | snv | 0.38 | 0.36 | 6 | |
rs903361 | 0.882 | 0.160 | 1 | 203122146 | intron variant | G/A;C | snv | 4 | |||
rs2072907 | 0.882 | 0.120 | 22 | 43936773 | intron variant | C/G | snv | 0.20 | 3 | ||
rs2290602 | 0.882 | 0.040 | 4 | 23824109 | intron variant | T/A;G | snv | 3 | |||
rs72563732 | 0.882 | 0.040 | 3 | 186854563 | synonymous variant | C/T | snv | 6.4E-05 | 2.6E-04 | 3 | |
rs738491 | 0.882 | 0.040 | 22 | 43958231 | intron variant | C/T | snv | 0.34 | 3 | ||
rs7643645 | 0.882 | 0.080 | 3 | 119806650 | intron variant | A/G | snv | 0.31 | 3 | ||
rs738408 | 0.925 | 0.120 | 22 | 43928850 | synonymous variant | C/T | snv | 0.28 | 0.22 | 10 | |
rs6601299 | 0.925 | 0.040 | 8 | 9327181 | intron variant | T/C | snv | 0.88 | 5 | ||
rs951599607 | 0.925 | 0.040 | 3 | 12434028 | missense variant | G/A | snv | 4 | |||
rs2235776 | 0.925 | 0.040 | 22 | 43982119 | intron variant | C/T | snv | 0.24 | 3 | ||
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 | ||
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 | ||
rs6006473 | 0.925 | 0.040 | 22 | 43997195 | intron variant | C/T | snv | 0.47 | 2 | ||
rs2126259 | 1.000 | 8 | 9327636 | intron variant | T/C | snv | 0.87 | 9 |