Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1454694 | 0.827 | 0.080 | 4 | 181276794 | intergenic variant | T/C | snv | 0.20 | 5 | ||
rs9295740 | 0.827 | 0.120 | 6 | 27721723 | intergenic variant | G/A | snv | 0.27 | 5 | ||
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs2032582 | 0.538 | 0.800 | 7 | 87531302 | missense variant | A/C;T | snv | 0.54; 3.8E-02 | 97 | ||
rs2231142 | 0.583 | 0.680 | 4 | 88131171 | missense variant | G/C;T | snv | 4.0E-06; 0.12 | 56 | ||
rs2241766 | 0.608 | 0.720 | 3 | 186853103 | synonymous variant | T/C;G | snv | 8.0E-06; 0.13 | 48 | ||
rs2070600 | 0.561 | 0.760 | 6 | 32183666 | missense variant | C/T | snv | 5.3E-02 | 3.6E-02 | 82 | |
rs4957014 | 0.752 | 0.160 | 5 | 287899 | intron variant | T/G | snv | 0.74 | 11 | ||
rs121434592 | 0.595 | 0.640 | 14 | 104780214 | missense variant | C/T | snv | 4.0E-06 | 54 | ||
rs778561687 | 0.851 | 0.080 | 19 | 40235953 | missense variant | C/A;T | snv | 4.0E-06; 4.0E-06 | 4 | ||
rs1057519698 | 0.827 | 0.120 | 2 | 29222347 | missense variant | A/G;T | snv | 8 | |||
rs1057519783 | 0.851 | 0.080 | 2 | 29220747 | missense variant | C/T | snv | 10 | |||
rs1057519784 | 0.827 | 0.080 | 2 | 29220765 | missense variant | G/T | snv | 7 | |||
rs1130409 | 0.555 | 0.720 | 14 | 20456995 | missense variant | T/A;C;G | snv | 4.0E-06; 4.0E-06; 0.42 | 72 | ||
rs2307486 | 0.790 | 0.240 | 14 | 20456045 | missense variant | A/G | snv | 7.4E-03 | 2.1E-03 | 7 | |
rs763375936 | 0.827 | 0.160 | 3 | 112532749 | missense variant | C/T | snv | 8.3E-06 | 7.0E-06 | 5 | |
rs772776695 | 0.827 | 0.160 | 3 | 112548576 | missense variant | T/A | snv | 4.0E-06 | 5 | ||
rs751688663 | 0.807 | 0.280 | 3 | 11340656 | missense variant | G/A | snv | 4.0E-06 | 7 | ||
rs189037 | 0.689 | 0.400 | 11 | 108223106 | 5 prime UTR variant | G/A | snv | 0.49 | 22 | ||
rs9535826 | 0.851 | 0.080 | 13 | 51991990 | intron variant | T/C;G | snv | 4 | |||
rs767935771 | 0.827 | 0.080 | 19 | 41259690 | missense variant | T/C | snv | 1.6E-05 | 5.6E-05 | 6 | |
rs1800469 | 0.547 | 0.760 | 19 | 41354391 | intron variant | A/G | snv | 0.69 | 78 | ||
rs3117582 | 0.716 | 0.440 | 6 | 31652743 | intron variant | T/G | snv | 7.1E-02 | 14 | ||
rs17655 | 0.597 | 0.560 | 13 | 102875652 | missense variant | G/C | snv | 0.28 | 0.30 | 52 | |
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 |