Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1360698171 | 0.851 | 0.080 | 1 | 182584103 | missense variant | T/C | snv | 4 | |||
rs149709822 | 0.882 | 0.080 | 19 | 50856335 | missense variant | G/A | snv | 4.0E-05 | 2.3E-04 | 4 | |
rs17036508 | 0.925 | 0.080 | 1 | 11195977 | 3 prime UTR variant | T/C | snv | 9.0E-02 | 4 | ||
rs17309872 | 0.925 | 0.080 | 20 | 34927985 | downstream gene variant | A/C;G;T | snv | 4 | |||
rs188140481 | 0.925 | 0.080 | 8 | 127179427 | non coding transcript exon variant | T/A;C | snv | 4 | |||
rs1902023 | 0.882 | 0.080 | 4 | 68670366 | missense variant | A/C | snv | 0.51 | 0.53 | 4 | |
rs1983891 | 0.925 | 0.080 | 6 | 41568689 | intron variant | C/T | snv | 0.35 | 4 | ||
rs198977 | 0.925 | 0.080 | 19 | 50878521 | missense variant | C/T | snv | 0.24 | 0.30 | 4 | |
rs266849 | 0.925 | 0.080 | 19 | 50845834 | intron variant | G/A | snv | 0.82 | 4 | ||
rs266882 | 0.925 | 0.080 | 19 | 50854757 | upstream gene variant | G/A | snv | 0.49 | 4 | ||
rs2705897 | 0.925 | 0.080 | 4 | 184631944 | splice region variant | T/G | snv | 0.64 | 0.73 | 4 | |
rs339331 | 0.882 | 0.080 | 6 | 116888889 | intron variant | T/C | snv | 0.28 | 4 | ||
rs367590266 | 0.925 | 0.080 | 6 | 52797630 | missense variant | T/C | snv | 1.2E-05 | 7.0E-06 | 4 | |
rs368952331 | 0.925 | 0.080 | 15 | 74722805 | missense variant | C/T | snv | 2.8E-05 | 6.3E-05 | 4 | |
rs4647603 | 0.925 | 0.080 | 4 | 184648576 | 5 prime UTR variant | C/T | snv | 0.11 | 4 | ||
rs544190 | 0.851 | 0.080 | 9 | 76763591 | intron variant | G/A | snv | 0.32 | 4 | ||
rs6763931 | 0.925 | 0.080 | 3 | 141383991 | intron variant | G/A | snv | 0.54 | 4 | ||
rs6983269 | 0.925 | 0.080 | 8 | 2741967 | intron variant | C/A;G;T | snv | 0.42 | 4 | ||
rs765521022 | 0.851 | 0.080 | 19 | 50858171 | missense variant | T/C | snv | 4 | |||
rs772893086 | 0.925 | 0.080 | 21 | 45176099 | missense variant | A/C;G;T | snv | 4.0E-06 | 4 | ||
rs775220785 | 0.925 | 0.080 | 7 | 99772615 | missense variant | C/T | snv | 8.0E-06 | 4 | ||
rs780354238 | 0.925 | 0.080 | 8 | 42369855 | missense variant | A/G | snv | 4.4E-06 | 4 | ||
rs822391 | 0.925 | 0.080 | 3 | 186846014 | intron variant | C/T | snv | 0.85 | 4 | ||
rs1045531 | 0.882 | 0.080 | 8 | 142682129 | synonymous variant | C/A | snv | 0.45 | 0.44 | 3 | |
rs10505474 | 0.925 | 0.080 | 8 | 127405259 | intron variant | T/C | snv | 0.47 | 3 |