Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1127313 | 1.000 | 0.120 | 1 | 154583949 | 3 prime UTR variant | G/A | snv | 0.41 | 1 | ||
rs1017134 | 0.925 | 0.120 | 7 | 35307237 | intergenic variant | G/A | snv | 0.47 | 2 | ||
rs1192691 | 0.925 | 0.120 | 10 | 36880367 | regulatory region variant | G/T | snv | 0.90 | 2 | ||
rs142091544 | 0.925 | 0.120 | 5 | 168286995 | upstream gene variant | C/T | snv | 2.1E-02 | 2 | ||
rs4286604 | 0.925 | 0.120 | 4 | 69576447 | intron variant | A/G | snv | 0.76 | 2 | ||
rs7501462 | 0.925 | 0.120 | 17 | 16974091 | upstream gene variant | A/G | snv | 0.31 | 2 | ||
rs1955513 | 0.925 | 0.120 | 14 | 32706736 | intron variant | T/G | snv | 0.11 | 2 | ||
rs927062 | 0.925 | 0.120 | 14 | 32625843 | intron variant | A/G | snv | 0.22 | 2 | ||
rs10788679 | 0.925 | 0.120 | 1 | 17590467 | intron variant | A/G | snv | 0.59 | 2 | ||
rs2256787 | 0.925 | 0.120 | 1 | 17566321 | intron variant | A/C | snv | 0.93 | 2 | ||
rs7572644 | 0.925 | 0.120 | 2 | 28097166 | intron variant | T/C | snv | 0.21 | 2 | ||
rs9609538 | 0.925 | 0.120 | 22 | 32413845 | upstream gene variant | T/C | snv | 0.34 | 2 | ||
rs1983383 | 0.925 | 0.120 | 2 | 30754766 | intron variant | C/A | snv | 0.39 | 2 | ||
rs41324349 | 0.925 | 0.120 | 7 | 2907529 | intron variant | G/A;C;T | snv | 2 | |||
rs3769827 | 0.925 | 0.120 | 2 | 201237962 | intron variant | A/G | snv | 0.42 | 2 | ||
rs17507066 | 0.925 | 0.120 | 22 | 28696732 | intron variant | C/T | snv | 7.0E-02 | 2 | ||
rs1413299 | 0.925 | 0.120 | 9 | 98998959 | intron variant | G/A;T | snv | 2 | |||
rs561841834 | 0.925 | 0.120 | 21 | 45468531 | synonymous variant | C/T | snv | 8.0E-06 | 2 | ||
rs114972508 | 0.925 | 0.120 | 7 | 55020815 | intron variant | T/C | snv | 1.4E-02 | 2 | ||
rs7053448 | 0.925 | 0.120 | X | 154964936 | intron variant | T/C | snv | 0.15 | 2 | ||
rs7058826 | 0.925 | 0.120 | X | 154966714 | intron variant | C/T | snv | 0.12 | 0.14 | 2 | |
rs17702471 | 0.925 | 0.120 | 13 | 93224864 | upstream gene variant | A/G | snv | 0.16 | 2 | ||
rs2190503 | 0.925 | 0.120 | 7 | 50674920 | intron variant | A/G;T | snv | 2 | |||
rs17427875 | 0.925 | 0.120 | 7 | 27185939 | non coding transcript exon variant | A/T | snv | 0.15 | 2 | ||
rs3745546 | 0.925 | 0.120 | 19 | 7211805 | intron variant | G/A;C | snv | 2 |