Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6746030 | 0.763 | 0.320 | 2 | 166242648 | missense variant | A/G | snv | 0.88 | 0.88 | 16 | |
rs121918799 | 0.752 | 0.120 | 2 | 166015636 | missense variant | G/C | snv | 1.7E-03 | 1.6E-03 | 14 | |
rs1559193213 | 0.807 | 0.160 | 2 | 166036149 | frameshift variant | -/G | delins | 11 | |||
rs121918622 | 0.790 | 0.080 | 2 | 165992332 | missense variant | C/A;T | snv | 4.0E-06 | 9 | ||
rs1553525325 | 0.807 | 0.120 | 2 | 166002716 | missense variant | A/T | snv | 9 | |||
rs121917984 | 0.790 | 0.080 | 2 | 166052869 | missense variant | G/A;C | snv | 8 | |||
rs3812718 | 0.776 | 0.240 | 2 | 166053034 | splice region variant | C/T | snv | 0.48 | 8 | ||
rs794726827 | 0.827 | 0.120 | 2 | 166054637 | splice donor variant | C/A;G;T | snv | 6 | |||
rs121918632 | 0.851 | 0.120 | 2 | 165996099 | missense variant | A/G | snv | 7.0E-06 | 5 | ||
rs121918807 | 0.851 | 0.080 | 2 | 165994275 | missense variant | G/A | snv | 7.2E-05 | 2.8E-05 | 5 | |
rs121918628 | 0.851 | 0.080 | 2 | 165998049 | missense variant | G/T | snv | 5 | |||
rs121918624 | 0.827 | 0.080 | 2 | 166052882 | stop gained | G/A | snv | 5 | |||
rs398123588 | 0.827 | 0.080 | 2 | 166039436 | missense variant | C/T | snv | 8.0E-06 | 5 | ||
rs121918775 | 0.827 | 0.080 | 2 | 166037886 | missense variant | G/A;T | snv | 5 | |||
rs121918805 | 0.925 | 0.080 | 2 | 166002660 | missense variant | C/A;T | snv | 2.0E-05 | 4 | ||
rs121918803 | 0.851 | 0.040 | 2 | 166009745 | missense variant | C/G | snv | 4 | |||
rs121917953 | 0.851 | 0.080 | 2 | 166054677 | missense variant | T/A | snv | 4 | |||
rs398123585 | 0.851 | 0.080 | 2 | 166043875 | stop gained | G/A;T | snv | 4.0E-06 | 4 | ||
rs794726775 | 0.882 | 0.040 | 2 | 166039420 | splice region variant | T/A | snv | 4 | |||
rs121917993 | 0.851 | 0.040 | 2 | 165994212 | missense variant | G/A | snv | 4 | |||
rs121917918 | 0.851 | 0.040 | 2 | 166058651 | missense variant | C/A;T | snv | 4 | |||
rs121917935 | 0.851 | 0.040 | 2 | 166054660 | missense variant | C/A;T | snv | 4 | |||
rs121917964 | 0.851 | 0.080 | 2 | 166073371 | missense variant | T/C | snv | 4 | |||
rs121917971 | 0.851 | 0.080 | 2 | 166037885 | missense variant | C/G;T | snv | 4 | |||
rs6432860 | 0.925 | 0.080 | 2 | 166041354 | synonymous variant | A/G;T | snv | 0.73; 4.0E-06 | 4 |