Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121912678 | 0.851 | 0.080 | 2 | 157774114 | missense variant | C/G;T | snv | 8 | |||
rs397514606 | 0.763 | 0.320 | 1 | 243695714 | missense variant | C/T | snv | 14 | |||
rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 116 | |
rs587777108 | 0.925 | 0.080 | 11 | 63646550 | missense variant | T/C | snv | 5 | |||
rs80338852 | 0.925 | 0.200 | 13 | 31317599 | stop gained | T/A;C | snv | 8.0E-06 | 3 | ||
rs806368 | 0.752 | 0.280 | 6 | 88140381 | 3 prime UTR variant | T/C | snv | 0.19 | 14 | ||
rs12720071 | 0.807 | 0.200 | 6 | 88141462 | 3 prime UTR variant | T/C | snv | 0.11 | 7 | ||
rs1234344050 | 2 | 188984825 | missense variant | C/G | snv | 4.0E-06 | 2 | ||||
rs387906617 | 2 | 207567506 | missense variant | A/G | snv | 2 | |||||
rs79204362 | 0.763 | 0.120 | 2 | 38071251 | missense variant | C/T | snv | 5.8E-03 | 1.7E-03 | 10 | |
rs57865060 | 0.827 | 0.160 | 2 | 38074704 | missense variant | C/T | snv | 1.1E-02 | 5.7E-03 | 6 | |
rs201968272 | 0.925 | 0.160 | 12 | 31089147 | missense variant | G/A | snv | 3 | |||
rs201405525 | 0.925 | 0.240 | 8 | 90044993 | missense variant | G/A;C | snv | 4.5E-04; 4.0E-06 | 3 | ||
rs764120087 | 22 | 41117439 | missense variant | G/A | snv | 8.0E-06 | 2 | ||||
rs7650466 | 0.851 | 0.200 | 3 | 89481208 | 3 prime UTR variant | C/T | snv | 0.23 | 7 | ||
rs1051740 | 0.592 | 0.760 | 1 | 225831932 | missense variant | T/C | snv | 0.32 | 0.27 | 56 | |
rs137854438 | 1.000 | 0.080 | 8 | 143728570 | stop gained | A/T | snv | 2 | |||
rs1801394 | 0.531 | 0.840 | 5 | 7870860 | missense variant | A/G | snv | 0.47 | 0.45 | 101 | |
rs1057519320 | 0.807 | 0.160 | 15 | 48444574 | missense variant | G/A | snv | 7 | |||
rs1057519321 | 0.807 | 0.160 | 5 | 128349391 | missense variant | C/A;T | snv | 7 | |||
rs142322800 | 1 | 161548502 | missense variant | T/C | snv | 1.5E-04 | 5.6E-05 | 1 | |||
rs1206736425 | 1 | 161626229 | missense variant | T/C | snv | 2 | |||||
rs77543610 | 0.667 | 0.560 | 10 | 121520160 | missense variant | G/C | snv | 28 | |||
rs121918502 | 0.790 | 0.160 | 10 | 121517351 | missense variant | G/C | snv | 9 | |||
rs121913483 | 0.649 | 0.560 | 4 | 1801841 | missense variant | C/A;G;T | snv | 4.2E-06; 1.3E-05 | 31 |