Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10510057 | 0.925 | 0.080 | 10 | 119551536 | intergenic variant | G/C | snv | 0.22 | 3 | ||
rs1937863 | 0.925 | 0.080 | 10 | 5009340 | intron variant | G/A;C;T | snv | 3 | |||
rs33990840 | 0.925 | 0.080 | 1 | 206116320 | missense variant | C/G;T | snv | 5.0E-02; 2.8E-05 | 3 | ||
rs139832701 | 0.925 | 0.080 | 3 | 8773124 | intron variant | T/G | snv | 0.13 | 3 | ||
rs553040076 | 0.925 | 0.080 | 19 | 10417700 | missense variant | T/A | snv | 4.5E-05 | 7.7E-05 | 3 | |
rs174696 | 0.925 | 0.080 | 22 | 19965653 | intron variant | C/A;T | snv | 3 | |||
rs1935062 | 0.882 | 0.080 | 13 | 105475787 | intron variant | A/C | snv | 0.32 | 3 | ||
rs4658966 | 0.925 | 0.080 | 1 | 231942868 | intron variant | T/C | snv | 0.19 | 3 | ||
rs977605156 | 0.925 | 0.080 | 16 | 3656127 | missense variant | G/A | snv | 7.0E-06 | 3 | ||
rs747052707 | 0.925 | 0.080 | 11 | 49192822 | missense variant | T/C | snv | 2.4E-05; 8.1E-06 | 3 | ||
rs2133450 | 0.925 | 0.080 | 3 | 7294765 | intron variant | A/C | snv | 0.38 | 3 | ||
rs6704393 | 0.925 | 0.080 | 1 | 162182266 | intron variant | C/A;T | snv | 3 | |||
rs1187329 | 0.925 | 0.080 | 9 | 84674365 | intron variant | A/G | snv | 0.52 | 3 | ||
rs1364647619 | 0.925 | 0.080 | 2 | 25161334 | missense variant | C/T | snv | 3 | |||
rs9376026 | 0.925 | 0.080 | 6 | 134281316 | intron variant | T/C | snv | 0.43 | 3 | ||
rs10997871 | 0.925 | 0.080 | 10 | 67913178 | intron variant | T/C | snv | 4.1E-03 | 3 | ||
rs5558 | 0.925 | 0.080 | 16 | 55699647 | missense variant | T/G | snv | 3 | |||
rs8192625 | 0.925 | 0.080 | 6 | 132571193 | missense variant | G/A | snv | 6.2E-02 | 7.8E-02 | 3 | |
rs7486220 | 0.925 | 0.080 | 12 | 56443632 | intron variant | C/T | snv | 3 | |||
rs12229394 | 0.925 | 0.080 | 12 | 71999134 | intron variant | G/A | snv | 0.29 | 3 | ||
rs12137417 | 0.925 | 0.080 | 1 | 231950407 | intron variant | G/A | snv | 0.17 | 3 | ||
rs2793094 | 0.925 | 0.080 | 1 | 231741236 | intron variant | G/A | snv | 0.97 | 3 | ||
rs10997875 | 0.882 | 0.080 | 10 | 67920067 | downstream gene variant | T/A;C | snv | 4 | |||
rs112025902 | 0.925 | 0.080 | 4 | 120232669 | intron variant | A/G;T | snv | 4 | |||
rs1491851 | 0.925 | 0.080 | 11 | 27731216 | intron variant | T/C;G | snv | 0.41 | 4 |