Source: CLINVAR
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs775097754 | 1.000 | 0.160 | 5 | 132378362 | intron variant | T/A | snv | 4.0E-05 | 1.4E-05 | 1 | |
rs1057519051 | 0.882 | 0.200 | 5 | 132390825 | stop gained | T/G | snv | 3 | |||
rs1057516765 | 1.000 | 0.160 | 5 | 132378475 | stop gained | C/G | snv | 1 | |||
rs1057518297 | 1.000 | 0.160 | 5 | 132390889 | stop gained | C/T | snv | 1 | |||
rs121908886 | 1.000 | 0.160 | 5 | 132387044 | stop gained | C/T | snv | 4.0E-05 | 4.9E-05 | 1 | |
rs121908887 | 1.000 | 0.160 | 5 | 132390838 | stop gained | -/A | delins | 1 | |||
rs121908893 | 1.000 | 0.160 | 5 | 132385435 | stop gained | C/A;T | snv | 5.3E-04; 1.2E-04 | 1 | ||
rs1253026669 | 1.000 | 0.160 | 5 | 132370224 | stop gained | C/G;T | snv | 1 | |||
rs1321705165 | 1.000 | 0.160 | 5 | 132370363 | stop gained | G/A;T | snv | 1.7E-05 | 7.0E-06 | 1 | |
rs1554085942 | 1.000 | 0.160 | 5 | 132370157 | stop gained | G/A | snv | 1 | |||
rs1554086010 | 1.000 | 0.160 | 5 | 132370333 | stop gained | C/T | snv | 1 | |||
rs1554088165 | 1.000 | 0.160 | 5 | 132390809 | stop gained | G/A | snv | 1 | |||
rs386134212 | 1.000 | 0.160 | 5 | 132387065 | stop gained | C/T | snv | 1.6E-05 | 1 | ||
rs72552722 | 1.000 | 0.160 | 5 | 132369984 | stop gained | C/G | snv | 8.0E-06 | 1 | ||
rs72552727 | 1.000 | 0.160 | 5 | 132378380 | stop gained | G/A | snv | 8.0E-06 | 1 | ||
rs763224132 | 1.000 | 0.160 | 5 | 132393683 | stop gained | C/A;G;T | snv | 4.0E-06; 1.2E-05 | 1 | ||
rs878853249 | 1.000 | 0.160 | 5 | 132385334 | stop gained | A/T | snv | 1 | |||
rs114269482 | 1.000 | 0.160 | 5 | 132385370 | missense variant | C/T | snv | 9.1E-05 | 1.8E-04 | 1 | |
rs11568520 | 1.000 | 0.160 | 5 | 132370023 | missense variant | C/G | snv | 1.2E-04 | 4.9E-05 | 1 | |
rs1178584184 | 1.000 | 0.160 | 5 | 132378412 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 1 | |
rs121908888 | 1.000 | 0.160 | 5 | 132384281 | missense variant | A/G | snv | 8.0E-06 | 7.0E-06 | 1 | |
rs121908889 | 1.000 | 0.160 | 5 | 132384155 | missense variant | G/A | snv | 4.4E-05 | 2.8E-05 | 1 | |
rs121908890 | 1.000 | 0.160 | 5 | 132384154 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
rs121908891 | 1.000 | 0.160 | 5 | 132390833 | missense variant | G/A | snv | 1.6E-05 | 2.1E-05 | 1 | |
rs144547521 | 1.000 | 0.160 | 5 | 132390830 | missense variant | C/T | snv | 8.0E-05 | 6.3E-05 | 1 |