Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11674595 | 0.763 | 0.200 | 2 | 101994530 | intron variant | T/C | snv | 0.22 | 13 | ||
rs4851527 | 0.790 | 0.160 | 2 | 102005914 | intron variant | A/G | snv | 0.63 | 7 | ||
rs719250 | 0.827 | 0.200 | 2 | 102007256 | intron variant | C/T | snv | 0.11 | 5 | ||
rs3218896 | 0.807 | 0.160 | 2 | 102015190 | intron variant | T/C;G | snv | 6 | |||
rs11568818 | 0.763 | 0.280 | 11 | 102530930 | upstream gene variant | T/A;C | snv | 15 | |||
rs77381814 | 0.882 | 0.080 | 14 | 103699410 | missense variant | C/T | snv | 1.5E-03 | 5.9E-03 | 3 | |
rs861539 | 0.519 | 0.680 | 14 | 103699416 | missense variant | G/A | snv | 0.29 | 0.30 | 104 | |
rs2255336 | 0.827 | 0.200 | 12 | 10379727 | missense variant | T/C | snv | 0.81 | 0.74 | 5 | |
rs807181 | 0.851 | 0.120 | X | 108090354 | intron variant | G/C;T | snv | 4 | |||
rs807183 | 0.851 | 0.120 | X | 108094263 | intron variant | G/A | snv | 0.51 | 4 | ||
rs1801516 | 0.627 | 0.400 | 11 | 108304735 | missense variant | G/A | snv | 0.11 | 0.11 | 39 | |
rs3787016 | 0.677 | 0.280 | 19 | 1090804 | intron variant | A/G | snv | 0.78 | 24 | ||
rs4938723 | 0.574 | 0.680 | 11 | 111511840 | intron variant | T/C | snv | 0.32 | 60 | ||
rs1800587 | 0.620 | 0.720 | 2 | 112785383 | upstream gene variant | G/A;C | snv | 0.32 | 43 | ||
rs1143630 | 0.827 | 0.160 | 2 | 112834078 | intron variant | T/A;G | snv | 5 | |||
rs1143627 | 0.605 | 0.760 | 2 | 112836810 | 5 prime UTR variant | G/A | snv | 0.56 | 47 | ||
rs16944 | 0.531 | 0.920 | 2 | 112837290 | upstream gene variant | A/G | snv | 0.57 | 92 | ||
rs997271472 | 1.000 | 0.080 | 5 | 112838434 | missense variant | G/A;T | snv | 4.0E-06 | 1 | ||
rs864622584 | 1.000 | 0.080 | 5 | 112838623 | missense variant | G/A | snv | 1 | |||
rs1110839 | 0.807 | 0.120 | 2 | 113236840 | non coding transcript exon variant | G/A;C;T | snv | 6 | |||
rs4848320 | 0.807 | 0.120 | 2 | 113253214 | intron variant | C/G;T | snv | 6 | |||
rs4570 | 0.882 | 0.080 | 8 | 116846150 | 3 prime UTR variant | G/A | snv | 0.70 | 4 | ||
rs2289937 | 0.882 | 0.080 | 8 | 116861572 | intron variant | G/A;C | snv | 4 | |||
rs4579555 | 0.882 | 0.080 | 8 | 116867092 | intron variant | A/G | snv | 4 | |||
rs1927911 | 0.658 | 0.640 | 9 | 117707776 | intron variant | A/G | snv | 0.62 | 28 |