Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1935 | 10 | 63168063 | missense variant | C/A;G;T | snv | 4.0E-06; 0.44 | 1 | ||||
rs41274072 | 10 | 63214396 | missense variant | T/C | snv | 2.9E-02 | 5.3E-02 | 1 | |||
rs10761731 | 10 | 63267850 | intron variant | A/T | snv | 0.38 | 6 | ||||
rs7896518 | 10 | 63344740 | intron variant | A/G | snv | 0.38 | 4 | ||||
rs10995477 | 10 | 63250912 | intron variant | T/C | snv | 0.43 | 4 | ||||
rs7916868 | 10 | 63229171 | intron variant | A/T | snv | 0.47 | 3 | ||||
rs7924036 | 10 | 63431885 | intron variant | G/A;T | snv | 3 | |||||
rs2393967 | 10 | 63373396 | intron variant | A/C | snv | 0.23 | 3 | ||||
rs10761741 | 1.000 | 0.040 | 10 | 63306426 | intron variant | G/T | snv | 0.38 | 3 | ||
rs7899503 | 10 | 63327708 | intron variant | C/G;T | snv | 2 | |||||
rs7082066 | 10 | 63239211 | intron variant | A/G | snv | 0.69 | 2 | ||||
rs3999089 | 10 | 63444048 | intron variant | A/G | snv | 0.41 | 2 | ||||
rs7902343 | 10 | 63245639 | intron variant | C/T | snv | 0.40 | 2 | ||||
rs75446656 | 1.000 | 0.080 | 10 | 63340256 | intron variant | C/A;T | snv | 1 | |||
rs10761765 | 10 | 63429213 | intron variant | A/G;T | snv | 1 | |||||
rs10761739 | 10 | 63302248 | intron variant | G/C | snv | 0.38 | 1 | ||||
rs10761733 | 10 | 63275024 | intron variant | T/A;C | snv | 1 | |||||
rs10995505 | 10 | 63331399 | intron variant | A/G;T | snv | 1 | |||||
rs6479901 | 10 | 63421016 | intron variant | C/A | snv | 0.66 | 1 | ||||
rs4745706 | 10 | 63399820 | intron variant | T/C | snv | 0.13 | 1 | ||||
rs10761751 | 10 | 63395125 | intron variant | A/G | snv | 0.42 | 1 | ||||
rs4379723 | 10 | 63203689 | intron variant | T/C | snv | 0.43 | 1 | ||||
rs7085862 | 10 | 63486687 | intron variant | T/G | snv | 0.66 | 1 | ||||
rs7075195 | 10 | 63290899 | intron variant | A/G | snv | 0.38 | 1 | ||||
rs7923609 | 10 | 63374062 | intron variant | A/G | snv | 0.43 | 1 |