Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519705 | 1.000 | 0.040 | 4 | 54727464 | missense variant | A/G | snv | 1 | |||
rs1057519706 | 1.000 | 0.040 | 4 | 54727474 | missense variant | T/G | snv | 1 | |||
rs1057519708 | 1.000 | 0.040 | 4 | 54728096 | missense variant | T/A;G | snv | 2 | |||
rs1057519710 | 0.695 | 0.280 | 4 | 54733166 | missense variant | G/C;T | snv | 22 | |||
rs1057519713 | 0.925 | 0.120 | 4 | 54736498 | missense variant | G/C | snv | 3 | |||
rs1057519718 | 0.925 | 0.160 | 7 | 140753355 | missense variant | CA/TC | mnv | 2 | |||
rs1057519720 | 0.851 | 0.080 | 7 | 140781602 | missense variant | CC/AA;GA | mnv | 4 | |||
rs1057519728 | 0.851 | 0.120 | 15 | 66435103 | missense variant | T/A;C;G | snv | 5 | |||
rs1057519729 | 0.827 | 0.080 | 15 | 66435113 | missense variant | A/C | snv | 6 | |||
rs1057519730 | 1.000 | 0.040 | 15 | 66436786 | missense variant | T/A;G | snv | 2 | |||
rs1057519731 | 0.925 | 0.040 | 15 | 66436816 | missense variant | G/C | snv | 2 | |||
rs1057519732 | 0.827 | 0.160 | 15 | 66436824 | missense variant | C/A;T | snv | 6 | |||
rs1057519733 | 1.000 | 0.040 | 15 | 66481793 | missense variant | G/A | snv | 1 | |||
rs1057519734 | 1.000 | 0.040 | 15 | 66485086 | missense variant | C/T | snv | 1 | |||
rs1057519735 | 1.000 | 0.040 | 15 | 66490577 | missense variant | A/C | snv | 1 | |||
rs1057519742 | 0.827 | 0.160 | 19 | 3118944 | missense variant | A/C;T | snv | 7 | |||
rs1057519804 | 1.000 | 0.040 | 14 | 104776711 | missense variant | G/T | snv | 2 | |||
rs1057519805 | 1.000 | 0.040 | 15 | 66436839 | missense variant | T/C | snv | 3 | |||
rs1057519806 | 0.882 | 0.200 | 19 | 4110583 | missense variant | T/C | snv | 3 | |||
rs1057519807 | 1.000 | 0.040 | 19 | 4110586 | missense variant | A/T | snv | 1 | |||
rs1057519808 | 1.000 | 0.040 | 19 | 4117543 | missense variant | T/G | snv | 2 | |||
rs1057519809 | 1.000 | 0.040 | 19 | 4117586 | missense variant | G/A;C | snv | 4.0E-06 | 1 | ||
rs1057519810 | 1.000 | 0.040 | 19 | 4117619 | missense variant | C/A;T | snv | 4.0E-06 | 1 | ||
rs1057519811 | 1.000 | 0.040 | 4 | 54274916 | missense variant | C/T | snv | 1 | |||
rs1057519812 | 1.000 | 0.040 | 4 | 54277977 | missense variant | T/C | snv | 1 |