Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1060499900 | 0.925 | 0.080 | 3 | 38551304 | missense variant | C/T | snv | 4.0E-06 | 1.4E-05 | 2 | |
rs12720452 | 0.882 | 0.120 | 3 | 38603758 | missense variant | C/T | snv | 2.9E-04 | 2.9E-04 | 5 | |
rs137854600 | 0.807 | 0.120 | 3 | 38551504 | missense variant | C/A;T | snv | 6 | |||
rs137854601 | 0.776 | 0.120 | 3 | 38551022 | stop gained | C/A;T | snv | 4.0E-06 | 10 | ||
rs137854602 | 0.925 | 0.080 | 3 | 38555664 | missense variant | G/A | snv | 5.6E-05 | 1.4E-05 | 5 | |
rs137854603 | 1.000 | 0.080 | 3 | 38550602 | missense variant | C/T | snv | 6.0E-05 | 2.8E-05 | 1 | |
rs137854604 | 0.882 | 0.120 | 3 | 38551243 | missense variant | G/A | snv | 1.6E-05 | 7.0E-06 | 3 | |
rs137854606 | 0.882 | 0.120 | 3 | 38604062 | missense variant | C/A | snv | 4 | |||
rs137854609 | 0.882 | 0.120 | 3 | 38581170 | missense variant | C/A;T | snv | 7.9E-05 | 3 | ||
rs137854611 | 0.882 | 0.120 | 3 | 38597787 | missense variant | G/A;C;T | snv | 4.0E-06 | 3 | ||
rs137854612 | 0.851 | 0.120 | 3 | 38560170 | missense variant | C/T | snv | 4 | |||
rs137854615 | 0.851 | 0.120 | 3 | 38550989 | missense variant | A/G | snv | 4 | |||
rs137854616 | 1.000 | 0.080 | 3 | 38566465 | missense variant | C/T | snv | 2.8E-05 | 7.0E-06 | 1 | |
rs137854617 | 0.882 | 0.120 | 3 | 38581002 | stop gained | C/A;T | snv | 1.1E-04 | 1.5E-04 | 3 | |
rs137854618 | 0.742 | 0.120 | 3 | 38566426 | missense variant | C/A;T | snv | 8.0E-06 | 15 | ||
rs137854620 | 1.000 | 0.080 | 3 | 38557268 | stop gained | C/T | snv | 1 | |||
rs1553605932 | 1.000 | 0.080 | 3 | 38622414 | stop gained | C/T | snv | 1 | |||
rs1559727990 | 1.000 | 0.080 | 3 | 38555727 | stop gained | G/A | snv | 1 | |||
rs1559729142 | 1.000 | 0.080 | 3 | 38556566 | missense variant | G/A | snv | 1 | |||
rs185492581 | 1.000 | 0.080 | 3 | 38630327 | stop gained | T/A;C | snv | 7.0E-06 | 1 | ||
rs185638763 | 0.882 | 0.120 | 3 | 38599001 | missense variant | G/A;T | snv | 1.2E-05 | 4 | ||
rs193922726 | 1.000 | 0.080 | 3 | 38551188 | missense variant | G/A;C | snv | 6.0E-05 | 1 | ||
rs199473045 | 0.925 | 0.120 | 3 | 38633228 | missense variant | C/A;T | snv | 8.0E-06; 2.5E-04 | 2 | ||
rs199473050 | 1.000 | 0.080 | 3 | 38633098 | missense variant | A/C | snv | 4.4E-05 | 1.4E-05 | 1 | |
rs199473051 | 0.925 | 0.120 | 3 | 38633058 | missense variant | C/T | snv | 2 |