Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1064725 | 1.000 | 0.120 | 19 | 44919304 | 3 prime UTR variant | T/G | snv | 3.4E-02 | 1 | ||
rs429358 | 0.590 | 0.600 | 19 | 44908684 | missense variant | T/C | snv | 0.14 | 0.16 | 66 | |
rs63749877 | 0.882 | 0.120 | 17 | 44351139 | frameshift variant | CACT/- | delins | 3 | |||
rs63751085 | 0.925 | 0.120 | 17 | 44350767 | frameshift variant | CA/- | del | 2 | |||
rs764232836 | 1.000 | 0.120 | 17 | 44349713 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
rs75932628 | 0.662 | 0.480 | 6 | 41161514 | missense variant | C/A;T | snv | 6.8E-05; 2.6E-03 | 28 | ||
rs143624519 | 0.724 | 0.240 | 17 | 45991484 | missense variant | G/A;T | snv | 1.5E-03; 1.2E-05 | 17 | ||
rs63750512 | 0.827 | 0.160 | 17 | 46024010 | missense variant | G/A;C | snv | 1.2E-05 | 6 | ||
rs63750301 | 0.827 | 0.120 | 14 | 73198052 | missense variant | C/T | snv | 4.0E-06 | 6 | ||
rs2075650 | 0.662 | 0.360 | 19 | 44892362 | intron variant | A/G | snv | 0.13 | 0.13 | 45 | |
rs157590 | 0.882 | 0.160 | 19 | 44895459 | intron variant | A/C | snv | 0.60 | 3 |