Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs119103263 | 0.827 | 0.240 | 1 | 11992659 | missense variant | C/T | snv | 19 | |||
rs121912854 | 0.851 | 0.200 | 3 | 48592915 | stop gained | G/A | snv | 1.2E-05 | 7.0E-06 | 16 | |
rs121912855 | 0.851 | 0.200 | 3 | 48575218 | missense variant | G/A | snv | 2.0E-05 | 7.0E-06 | 16 | |
rs765243124 | 0.827 | 0.160 | 10 | 104033953 | frameshift variant | CTCT/- | delins | 4.0E-06 | 14 | ||
rs121912856 | 0.732 | 0.120 | 3 | 48593538 | missense variant | T/C | snv | 3.2E-05 | 9.1E-05 | 13 | |
rs1114167422 | 0.776 | 0.320 | X | 154773148 | missense variant | A/G | snv | 11 | |||
rs780261665 | 0.827 | 0.200 | 3 | 48590258 | stop gained | G/A | snv | 2.0E-05 | 1.4E-05 | 9 | |
rs121912834 | 0.827 | 0.120 | 3 | 48572941 | missense variant | C/G;T | snv | 4.0E-06 | 6 | ||
rs141480813 | 0.882 | 0.080 | 21 | 44289752 | missense variant | A/T | snv | 2.8E-05 | 1.5E-04 | 4 |