Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12527379 | 1.000 | 0.080 | 6 | 131958700 | intron variant | G/A | snv | 0.31 | 1 | ||
rs1371367785 | 1.000 | 0.080 | 11 | 70206265 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
rs17878467 | 0.925 | 0.080 | 17 | 78214076 | upstream gene variant | C/G;T | snv | 6 | |||
rs60745952 | 0.925 | 0.080 | 4 | 148827842 | intron variant | T/C | snv | 0.13 | 6 | ||
rs4135113 | 0.925 | 0.080 | 12 | 103982915 | missense variant | G/A;C;T | snv | 4.7E-02 | 5 | ||
rs10222633 | 0.925 | 0.080 | 3 | 122258079 | intron variant | G/A | snv | 0.45 | 4 | ||
rs10934578 | 0.925 | 0.080 | 3 | 122258435 | intron variant | G/T | snv | 0.30 | 4 | ||
rs12591359 | 0.925 | 0.080 | 15 | 51247171 | intron variant | G/A | snv | 0.41 | 4 | ||
rs2770150 | 0.925 | 0.080 | 9 | 117700861 | upstream gene variant | A/G | snv | 0.22 | 4 | ||
rs7987649 | 0.925 | 0.080 | 13 | 28320278 | intron variant | A/G | snv | 0.35 | 4 | ||
rs1017621656 | 0.925 | 0.080 | 19 | 41352923 | missense variant | A/C;G | snv | 1.9E-05 | 3 | ||
rs1057519822 | 0.925 | 0.080 | 15 | 66481818 | missense variant | T/A | snv | 3 | |||
rs1440032367 | 0.925 | 0.080 | 6 | 33189169 | missense variant | G/C | snv | 7.0E-06 | 3 | ||
rs187960998 | 0.925 | 0.080 | 15 | 31065098 | mature miRNA variant | C/T | snv | 1.2E-05 | 6.3E-05 | 3 | |
rs352144 | 0.925 | 0.080 | 3 | 52227452 | intron variant | T/G | snv | 3.7E-02 | 3 | ||
rs4562 | 0.925 | 0.080 | 17 | 7260420 | missense variant | A/G | snv | 0.65 | 0.70 | 3 | |
rs4648110 | 0.925 | 0.080 | 4 | 102612664 | intron variant | T/A | snv | 0.22 | 3 | ||
rs63751701 | 0.925 | 0.080 | 3 | 36993663 | stop gained | G/A;T | snv | 3 | |||
rs760891242 | 0.925 | 0.080 | 3 | 14168309 | missense variant | G/C | snv | 4.0E-06 | 7.0E-06 | 3 | |
rs774904310 | 0.925 | 0.080 | 9 | 21971055 | frameshift variant | C/- | delins | 3 | |||
rs9869263 | 0.925 | 0.080 | 3 | 190312891 | synonymous variant | A/C;G;T | snv | 8.0E-06; 0.83; 4.0E-06 | 3 | ||
rs10450310 | 0.925 | 0.080 | 10 | 52764898 | downstream gene variant | G/A | snv | 0.29 | 2 | ||
rs1060503118 | 0.925 | 0.080 | 7 | 5987422 | missense variant | C/T | snv | 2 | |||
rs10958713 | 0.925 | 0.080 | 8 | 42323198 | intron variant | C/T | snv | 0.28 | 2 | ||
rs11625206 | 0.925 | 0.080 | 14 | 70727436 | 3 prime UTR variant | C/T | snv | 0.26 | 2 |