Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs374512193 | 0.925 | 0.120 | 8 | 42838177 | missense variant | T/C | snv | 5.2E-05 | 5.6E-05 | 4 | |
rs1064797344 | 1.000 | 0.080 | 8 | 42843033 | missense variant | G/A | snv | 1 | |||
rs1131691345 | 1.000 | 0.080 | 8 | 42838099 | stop gained | G/A;C | snv | 1 | |||
rs118204013 | 1.000 | 0.080 | 8 | 42839212 | missense variant | A/G | snv | 1 | |||
rs138918468 | 1.000 | 0.080 | 8 | 42838108 | missense variant | C/T | snv | 2.4E-05 | 2.8E-05 | 1 | |
rs1554599616 | 1.000 | 0.080 | 8 | 42838315 | stop gained | G/A | snv | 1 | |||
rs1554599712 | 1.000 | 0.080 | 8 | 42839322 | frameshift variant | T/- | delins | 1 | |||
rs1554599983 | 1.000 | 0.080 | 8 | 42843088 | stop gained | G/A | snv | 1 | |||
rs1563644456 | 1.000 | 0.080 | 8 | 42838298 | frameshift variant | -/G | delins | 1 | |||
rs1563644810 | 1.000 | 0.080 | 8 | 42839244 | inframe deletion | TTG/- | delins | 1 | |||
rs1563646198 | 1.000 | 0.080 | 8 | 42843093 | start lost | A/G | snv | 1 | |||
rs267607111 | 1.000 | 0.080 | 8 | 42839187 | missense variant | T/C | snv | 7.0E-06 | 1 | ||
rs267607112 | 1.000 | 0.080 | 8 | 42843070 | missense variant | C/A | snv | 1 | |||
rs372080941 | 1.000 | 0.080 | 8 | 42839215 | missense variant | T/A;C | snv | 2.8E-05 | 1 | ||
rs377725442 | 1.000 | 0.080 | 8 | 42838030 | missense variant | C/T | snv | 4.0E-06 | 3.5E-05 | 1 | |
rs387907176 | 1.000 | 0.080 | 8 | 42843025 | missense variant | T/C | snv | 1 | |||
rs387907177 | 1.000 | 0.080 | 8 | 42843027 | missense variant | T/G | snv | 1 | |||
rs759392096 | 1.000 | 0.080 | 8 | 42838083 | missense variant | T/C | snv | 8.0E-06 | 1 | ||
rs766483829 | 1.000 | 0.080 | 8 | 42843045 | missense variant | T/C | snv | 2.8E-05 | 1 | ||
rs767519301 | 1.000 | 0.080 | 8 | 42838098 | missense variant | C/T | snv | 1.2E-05 | 1 | ||
rs767952378 | 1.000 | 0.080 | 8 | 42839367 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
rs768017019 | 1.000 | 0.080 | 8 | 42839206 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 1 | |
rs769988455 | 1.000 | 0.080 | 8 | 42838197 | missense variant | T/C | snv | 1.6E-05 | 1.4E-05 | 1 | |
rs950435041 | 1.000 | 0.080 | 8 | 42838209 | missense variant | A/G | snv | 1.6E-05 | 2.1E-05 | 1 |