Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs910532454 | 0.882 | 0.080 | 2 | 136115453 | missense variant | C/A;T | snv | 4.0E-06 | 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 | |||
rs11536898 | 0.882 | 0.080 | 9 | 117717932 | 3 prime UTR variant | C/A | snv | 0.14 | 3 | ||
rs11986055 | 0.882 | 0.080 | 8 | 42277660 | intron variant | A/C;G | snv | 3 | |||
rs121913538 | 0.882 | 0.080 | 12 | 25245328 | missense variant | C/A;G | snv | 3 | |||
rs1440032367 | 0.925 | 0.080 | 6 | 33189169 | missense variant | G/C | snv | 7.0E-06 | 3 | ||
rs147198552 | 0.882 | 0.080 | 2 | 136115450 | missense variant | C/T | snv | 1.2E-05 | 7.0E-06 | 3 | |
rs187960998 | 0.925 | 0.080 | 15 | 31065098 | mature miRNA variant | C/T | snv | 1.2E-05 | 6.3E-05 | 3 | |
rs2059691 | 0.882 | 0.080 | 2 | 178437157 | intron variant | A/G | snv | 0.72 | 3 | ||
rs2189517 | 0.882 | 0.080 | 14 | 68536271 | intron variant | A/G | snv | 0.49 | 3 | ||
rs230490 | 0.882 | 0.080 | 4 | 102466262 | downstream gene variant | G/A | snv | 0.34 | 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 | |||
rs6474387 | 0.882 | 0.080 | 8 | 42328734 | intron variant | T/C | snv | 0.76 | 3 | ||
rs6598964 | 0.882 | 0.080 | 1 | 26419836 | intron variant | A/G | snv | 0.67 | 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 | |||
rs7911488 | 0.882 | 0.080 | 10 | 103394332 | 5 prime UTR variant | A/G | snv | 0.34 | 0.26 | 3 | |
rs9869263 | 0.925 | 0.080 | 3 | 190312891 | synonymous variant | A/C;G;T | snv | 8.0E-06; 0.83; 4.0E-06 | 3 | ||
rs997476 | 0.882 | 0.080 | 4 | 102620848 | downstream gene variant | G/T | snv | 4.3E-02 | 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 |