Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1131691021 | 0.716 | 0.120 | 17 | 7675097 | missense variant | A/C;G | snv | 21 | |||
rs111033565 | 0.742 | 0.120 | 7 | 142751938 | missense variant | G/A | snv | 1.2E-05 | 11 | ||
rs267606982 | 0.742 | 0.120 | 7 | 142751938 | missense variant | GC/AT | mnv | 11 | |||
rs1049074086 | 0.925 | 0.120 | 11 | 1759567 | missense variant | A/G | snv | 7.0E-06 | 9 | ||
rs12413624 | 0.851 | 0.120 | 10 | 118519432 | intergenic variant | T/A | snv | 0.34 | 5 | ||
rs2239186 | 0.882 | 0.120 | 12 | 47875627 | intron variant | A/C;G | snv | 0.17 | 5 | ||
rs80358683 | 0.851 | 0.120 | 13 | 32338880 | stop gained | C/T | snv | 5 | |||
rs9502893 | 0.827 | 0.120 | 6 | 1339954 | intergenic variant | C/G;T | snv | 5 | |||
rs1176026649 | 0.851 | 0.120 | 4 | 168921582 | missense variant | C/T | snv | 7.2E-06 | 4 | ||
rs199976573 | 0.925 | 0.120 | 4 | 88132618 | missense variant | C/T | snv | 6.4E-05 | 5.6E-05 | 4 | |
rs2229629 | 0.882 | 0.120 | 2 | 74889400 | missense variant | G/A | snv | 6.0E-02 | 0.18 | 4 | |
rs4759313 | 0.851 | 0.120 | 12 | 53965290 | intron variant | T/A | snv | 0.51 | 4 | ||
rs56053615 | 0.851 | 0.120 | 3 | 9751845 | missense variant | G/A;T | snv | 3.4E-04; 4.0E-06 | 4 | ||
rs78303930 | 0.925 | 0.120 | 1 | 156670593 | missense variant | C/A;G | snv | 4.0E-06; 2.4E-03 | 4 | ||
rs786203926 | 0.882 | 0.120 | 11 | 108227678 | synonymous variant | T/C | snv | 4 | |||
rs9564966 | 0.851 | 0.120 | 13 | 73322084 | intergenic variant | A/G | snv | 0.52 | 4 | ||
rs980303898 | 0.851 | 0.120 | 2 | 162147479 | missense variant | T/C | snv | 8.0E-06 | 7.0E-06 | 4 | |
rs11644322 | 0.925 | 0.120 | 16 | 79005703 | intron variant | C/T | snv | 0.22 | 3 | ||
rs12029406 | 0.882 | 0.120 | 1 | 199936700 | intergenic variant | C/T | snv | 0.36 | 3 | ||
rs1209809979 | 0.925 | 0.120 | 1 | 45568989 | missense variant | A/G | snv | 4.0E-06 | 3 | ||
rs1370041903 | 0.925 | 0.120 | 6 | 161350185 | stop gained | G/A | snv | 3 | |||
rs139599857 | 0.882 | 0.120 | 19 | 43545922 | missense variant | C/G | snv | 1.6E-05 | 2.1E-05 | 3 | |
rs150495372 | 0.925 | 0.120 | 4 | 99313834 | missense variant | C/T | snv | 3.7E-04 | 3 | ||
rs1517037 | 0.882 | 0.120 | 18 | 59211042 | intergenic variant | C/T | snv | 0.23 | 3 | ||
rs1537373 | 0.925 | 0.120 | 9 | 22103342 | intron variant | T/G | snv | 0.63 | 3 |