Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2075650 | 0.662 | 0.360 | 19 | 44892362 | intron variant | A/G | snv | 0.13 | 0.13 | 20 | |
rs157580 | 0.882 | 0.160 | 19 | 44892009 | intron variant | G/A | snv | 0.69 | 11 | ||
rs1160985 | 1.000 | 0.080 | 19 | 44900155 | intron variant | C/T | snv | 0.52 | 5 | ||
rs8106922 | 1.000 | 0.080 | 19 | 44898409 | intron variant | A/G | snv | 0.36 | 4 | ||
rs157582 | 0.851 | 0.160 | 19 | 44892962 | intron variant | C/T | snv | 0.24 | 0.29 | 3 | |
rs34404554 | 1.000 | 0.080 | 19 | 44892652 | intron variant | C/G | snv | 0.12 | 2 | ||
rs741780 | 1.000 | 0.080 | 19 | 44901174 | intron variant | T/C | snv | 0.47 | 0.52 | 1 | |
rs760136 | 1.000 | 0.080 | 19 | 44900601 | intron variant | A/G | snv | 0.52 | 1 | ||
rs157590 | 0.882 | 0.160 | 19 | 44895459 | intron variant | A/C | snv | 0.60 | 1 | ||
rs11668327 | 1.000 | 0.080 | 19 | 44895376 | intron variant | G/C | snv | 0.12 | 1 | ||
rs61679753 | 1.000 | 0.080 | 19 | 44897490 | intron variant | T/A | snv | 5.6E-02 | 1 | ||
rs76366838 | 19 | 44896639 | intron variant | G/A;T | snv | 1 | |||||
rs11556505 | 0.925 | 0.080 | 19 | 44892887 | synonymous variant | C/T | snv | 0.13 | 0.13 | 2 | |
rs157581 | 0.925 | 0.080 | 19 | 44892457 | synonymous variant | T/C | snv | 0.25 | 0.29 | 1 | |
rs10119 | 0.925 | 0.080 | 19 | 44903416 | 3 prime UTR variant | G/A | snv | 0.28 | 3 | ||
rs1038026 | 1.000 | 0.080 | 19 | 44901805 | 3 prime UTR variant | A/G;T | snv | 1 | |||
rs1038025 | 1.000 | 0.080 | 19 | 44901715 | 3 prime UTR variant | T/C;G | snv | 1 | |||
rs405697 | 1.000 | 0.080 | 19 | 44901434 | 3 prime UTR variant | A/G;T | snv | 1 |