Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10878232 | 1.000 | 0.080 | 12 | 65128867 | intergenic variant | T/A;C;G | snv | 1 | |||
rs11674251 | 1.000 | 0.080 | 2 | 20016748 | upstream gene variant | T/C | snv | 0.18 | 1 | ||
rs12000445 | 1.000 | 0.080 | 9 | 23426273 | intron variant | A/G | snv | 0.18 | 1 | ||
rs1209950 | 1.000 | 0.080 | 21 | 38801604 | upstream gene variant | C/T | snv | 0.30 | 1 | ||
rs1414493 | 1.000 | 0.080 | 1 | 241523216 | upstream gene variant | A/G | snv | 0.62 | 1 | ||
rs1957860 | 1.000 | 0.080 | 14 | 53962637 | upstream gene variant | C/T | snv | 0.51 | 1 | ||
rs4743325 | 1.000 | 0.080 | 9 | 99087445 | intergenic variant | G/T | snv | 0.24 | 1 | ||
rs6122390 | 1.000 | 0.080 | 20 | 63173912 | intron variant | C/T | snv | 0.27 | 1 | ||
rs7629386 | 1.000 | 0.080 | 3 | 40925416 | regulatory region variant | C/T | snv | 0.30 | 1 | ||
rs9660710 | 1.000 | 0.080 | 1 | 1163962 | upstream gene variant | A/C;T | snv | 1 | |||
rs969088 | 1.000 | 0.080 | 5 | 26389153 | intron variant | G/C | snv | 9.9E-02 | 1 | ||
rs9909179 | 1.000 | 0.080 | 17 | 13140986 | regulatory region variant | T/C | snv | 0.37 | 1 | ||
rs750443908 | 1.000 | 0.080 | 10 | 50859904 | missense variant | C/A;T | snv | 6.0E-05; 8.0E-06 | 1 | ||
rs2725264 | 1.000 | 0.080 | 4 | 88104957 | intron variant | C/T | snv | 0.70 | 1 | ||
rs4148149 | 1.000 | 0.080 | 4 | 88141133 | intron variant | T/G | snv | 0.42 | 1 | ||
rs768122549 | 1.000 | 0.080 | 20 | 34260386 | synonymous variant | C/G;T | snv | 4.0E-06 | 1 | ||
rs754845817 | 1.000 | 0.080 | 12 | 111790494 | missense variant | G/A | snv | 1.6E-05 | 1.4E-05 | 1 | |
rs550608288 | 1.000 | 0.080 | 2 | 29717646 | missense variant | T/C | snv | 5.2E-05 | 1 | ||
rs958335893 | 1.000 | 0.080 | 2 | 29193478 | missense variant | C/T | snv | 1 | |||
rs919968 | 1.000 | 0.080 | 15 | 79205004 | intron variant | T/A;G | snv | 1 | |||
rs41997 | 1.000 | 0.080 | 7 | 118351841 | intron variant | A/G | snv | 0.27 | 1 | ||
rs228590 | 1.000 | 0.080 | 11 | 108225414 | 5 prime UTR variant | A/G | snv | 0.52 | 1 | ||
rs170548 | 1.000 | 0.080 | 11 | 108364109 | intron variant | A/C;T | snv | 1 | |||
rs9526814 | 1.000 | 0.080 | 13 | 51965390 | intron variant | T/G | snv | 0.35 | 1 | ||
rs17878624 | 1.000 | 0.080 | 17 | 78224418 | 3 prime UTR variant | G/A | snv | 5.0E-04 | 1 |