Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11540478 | 0.851 | 0.080 | 15 | 90085305 | synonymous variant | G/A;C | snv | 3.5E-02; 6.4E-06 | 4 | ||
rs1171287261 | 0.851 | 0.080 | 7 | 55191839 | missense variant | G/A | snv | 4 | |||
rs11778573 | 0.851 | 0.080 | 8 | 133216687 | intron variant | T/G | snv | 0.59 | 4 | ||
rs1226168728 | 0.851 | 0.080 | 19 | 45398021 | missense variant | G/C | snv | 7.0E-06 | 4 | ||
rs1362623672 | 0.851 | 0.080 | 19 | 45421317 | missense variant | G/C | snv | 1.4E-05 | 4 | ||
rs1564483 | 1.000 | 0.080 | 18 | 63127421 | 3 prime UTR variant | C/T | snv | 0.22 | 4 | ||
rs1878022 | 0.851 | 0.080 | 12 | 108305255 | intron variant | C/T | snv | 0.70 | 4 | ||
rs2293347 | 0.851 | 0.080 | 7 | 55201223 | synonymous variant | C/T | snv | 0.14 | 9.5E-02 | 4 | |
rs2977536 | 0.851 | 0.080 | 8 | 133207034 | intron variant | G/C | snv | 0.36 | 4 | ||
rs3805213 | 0.851 | 0.080 | 4 | 139044570 | intron variant | C/T | snv | 0.23 | 4 | ||
rs4065 | 0.851 | 0.080 | 10 | 73916706 | 3 prime UTR variant | C/T | snv | 0.51 | 4 | ||
rs4978754 | 0.851 | 0.080 | 9 | 108884801 | intron variant | T/C | snv | 0.92 | 4 | ||
rs662959 | 0.851 | 0.080 | 3 | 159983443 | intron variant | G/A | snv | 0.16 | 4 | ||
rs677844 | 0.851 | 0.080 | 1 | 12184261 | intron variant | T/C | snv | 0.22 | 4 | ||
rs7170924 | 0.851 | 0.080 | 15 | 81290798 | intron variant | G/T | snv | 0.30 | 4 | ||
rs727502902 | 0.882 | 0.080 | 7 | 140753338 | inframe insertion | -/TAG | delins | 4.0E-06 | 4 | ||
rs750758481 | 0.851 | 0.080 | 5 | 132603476 | missense variant | T/C | snv | 8.0E-06 | 7.0E-06 | 4 | |
rs751306825 | 0.925 | 0.080 | 2 | 29220759 | missense variant | G/A;T | snv | 4.0E-06 | 4 | ||
rs753254929 | 0.851 | 0.080 | 14 | 20455915 | missense variant | G/A;C | snv | 1.6E-05 | 4 | ||
rs7631358 | 0.851 | 0.080 | 3 | 189630622 | upstream gene variant | G/A | snv | 0.13 | 4 | ||
rs778561687 | 0.851 | 0.080 | 19 | 40235953 | missense variant | C/A;T | snv | 4.0E-06; 4.0E-06 | 4 | ||
rs863225283 | 0.925 | 0.080 | 2 | 29213993 | missense variant | A/C | snv | 4 | |||
rs928508 | 0.851 | 0.080 | 1 | 40757742 | intron variant | G/A;T | snv | 0.50 | 4 | ||
rs9535826 | 0.851 | 0.080 | 13 | 51991990 | intron variant | T/C;G | snv | 4 | |||
rs967591 | 0.851 | 0.080 | 19 | 45406676 | 5 prime UTR variant | G/A;C;T | snv | 0.22; 6.7E-06 | 4 |