PHLDB3
pleckstrin homology like domain family B member 3
Summary
Enables enzyme binding activity. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants59 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs372753592 | 19:43,979,632 | G/A | — | uncertain significance |
| rs141470268 | 19:43,981,360 | A/T | intron variant | — |
| rs757119202 | 19:43,982,206 | G/T | — | uncertain significance |
| rs565828916 | 19:43,982,213 | G/A | — | benign |
| rs1599930631 | 19:43,982,234 | C/T | — | uncertain significance |
| rs371843053 | 19:43,982,272 | G/T | — | uncertain significance |
| rs187491146 | 19:43,982,488 | G/C | intron variant | — |
| rs2513531272 | 19:43,983,535 | A/T | — | uncertain significance |
| rs757672037 | 19:43,983,607 | T/C | — | uncertain significance |
| rs1343945971 | 19:43,983,654 | G/T | — | uncertain significance |
| rs1133929 | 19:43,983,740 | T/G | — | likely benign |
| rs538624470 | 19:43,983,741 | G/A | — | uncertain significance |
| rs767454599 | 19:43,983,753 | G/T | — | likely benign |
| rs201337364 | 19:43,990,438 | G/A | — | uncertain significance |
| rs763371566 | 19:43,990,449 | C/A | — | uncertain significance |
| rs199522851 | 19:43,990,762 | C/T | — | uncertain significance |
| rs200865883 | 19:43,990,789 | G/A | — | uncertain significance |
| rs200233313 | 19:43,990,796 | C/T | — | uncertain significance |
| rs764189221 | 19:43,990,844 | C/T | — | uncertain significance |
| rs563295063 | 19:43,990,942 | G/A | — | uncertain significance |
| rs753664131 | 19:43,991,002 | G/T | — | uncertain significance |
| rs758032268 | 19:43,991,014 | C/T | — | uncertain significance |
| rs141588036 | 19:43,991,019 | G/T | — | likely benign |
| rs761687416 | 19:43,991,199 | C/T | — | uncertain significance |
| rs200551584 | 19:43,991,203 | G/A | — | uncertain significance |
| rs933102247 | 19:43,991,205 | G/T | — | uncertain significance |
| rs1348282528 | 19:43,991,227 | C/T | — | uncertain significance |
| rs749748998 | 19:43,991,231 | C/A | — | uncertain significance |
| rs546205925 | 19:43,991,239 | G/A | — | uncertain significance |
| rs1212839617 | 19:43,991,247 | C/A | — | uncertain significance |
| rs142727946 | 19:43,991,255 | C/G | — | uncertain significance |
| rs35107209 | 19:43,992,228 | C/G | intron variant | — |
| rs182026781 | 19:43,996,018 | C/T | intron variant | — |
| rs11671471 | 19:43,996,732 | G/A | intron variant | — |
| rs142679800 | 19:43,998,863 | G/C | — | benign |
| rs146907529 | 19:43,999,403 | C/T | — | benign |
| rs1125031 | 19:43,999,432 | A/G | — | benign |
| rs767593402 | 19:43,999,451 | G/A | — | uncertain significance |
| rs752680293 | 19:43,999,658 | C/G | — | uncertain significance |
| rs375933397 | 19:43,999,693 | C/T | — | uncertain significance |
| rs780494557 | 19:43,999,754 | G/A | — | uncertain significance |
| rs1156784860 | 19:44,001,276 | C/A | — | uncertain significance |
| rs200488755 | 19:44,001,359 | G/A | — | uncertain significance |
| rs150671965 | 19:44,001,363 | C/G | — | uncertain significance |
| rs531681888 | 19:44,001,950 | C/A | — | uncertain significance |
| rs146405145 | 19:44,001,970 | C/T | — | uncertain significance |
| rs139512157 | 19:44,001,971 | G/A | — | uncertain significance |
| rs376140257 | 19:44,002,003 | C/T | — | uncertain significance |
| rs749023114 | 19:44,002,018 | C/T | — | uncertain significance |
| rs377471313 | 19:44,002,019 | G/A | — | uncertain significance |
| rs144873749 | 19:44,002,394 | G/A | intron variant | — |
| rs2513582991 | 19:44,005,944 | C/T | — | uncertain significance |
| rs751407231 | 19:44,006,278 | C/A | — | uncertain significance |
| rs76853904 | 19:44,006,342 | C/T | — | likely benign |
| rs755627272 | 19:44,006,396 | G/C | — | likely benign |
| rs868637101 | 19:44,006,432 | C/T | — | uncertain significance |
| rs1362475970 | 19:44,008,183 | C/G | — | uncertain significance |
| rs147649189 | 19:44,008,221 | G/A | — | uncertain significance |
| rs780882753 | 19:44,008,254 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.