HS1BP3
HCLS1 binding protein 3
Summary
The protein encoded by this gene shares similarity with mouse Hs1bp3, an Hcls1/Hs1-interacting protein that may be involved in lymphocyte activation. [provided by RefSeq, Jul 2008]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1363429794 | 2:20,818,793 | A/G | — | uncertain significance |
| rs775987515 | 2:20,818,801 | C/A | — | uncertain significance |
| rs1462318822 | 2:20,818,812 | T/A | — | uncertain significance |
| rs111886213 | 2:20,818,816 | G/A | — | benign |
| rs139786951 | 2:20,818,882 | G/T | — | likely benign |
| rs2465448751 | 2:20,819,001 | C/T | — | uncertain significance |
| rs371998609 | 2:20,823,676 | G/T | — | likely benign |
| rs781479642 | 2:20,823,695 | G/A | — | uncertain significance |
| rs774794763 | 2:20,823,714 | C/T | — | uncertain significance |
| rs369503300 | 2:20,823,720 | C/T | — | uncertain significance |
| rs372329576 | 2:20,823,725 | G/A | — | uncertain significance |
| rs867848929 | 2:20,823,746 | A/G | — | uncertain significance |
| rs746318677 | 2:20,823,762 | C/T | — | uncertain significance |
| rs370938945 | 2:20,824,578 | T/C | — | uncertain significance |
| rs183381441 | 2:20,824,579 | C/T | — | uncertain significance |
| rs566011144 | 2:20,824,602 | G/A | — | likely benign |
| rs144429298 | 2:20,824,605 | G/A | — | conflicting classifications of pathogenicity |
| rs148439062 | 2:20,824,613 | T/G | — | uncertain significance |
| rs775357357 | 2:20,824,641 | G/T | — | uncertain significance |
| rs62122090 | 2:20,828,309 | C/T | intron variant | — |
| rs2465514586 | 2:20,838,251 | C/T | — | uncertain significance |
| rs144903305 | 2:20,838,277 | G/A | — | likely benign |
| rs761650430 | 2:20,840,781 | A/T | — | uncertain significance |
| rs1322449879 | 2:20,840,789 | C/T | — | uncertain significance |
| rs77551133 | 2:20,840,823 | G/A | — | benign |
| rs746489178 | 2:20,840,826 | T/A | — | uncertain significance |
| rs144812348 | 2:20,840,850 | C/A | — | uncertain significance |
| rs1288062932 | 2:20,840,858 | G/T | — | uncertain significance |
| rs77941615 | 2:20,840,864 | G/C | — | uncertain significance |
| rs765692930 | 2:20,840,883 | C/T | — | uncertain significance |
| rs139333579 | 2:20,840,933 | T/G | — | uncertain significance |
| rs115108428 | 2:20,845,095 | C/T | splice region variant | — |
| rs766908220 | 2:20,845,134 | G/A | — | uncertain significance |
| rs2465539512 | 2:20,845,171 | T/A | — | uncertain significance |
| rs148722602 | 2:20,845,183 | C/T | — | uncertain significance |
| rs749637149 | 2:20,845,207 | G/A | — | uncertain significance |
| rs140634250 | 2:20,845,213 | C/T | — | uncertain significance |
| rs1310783274 | 2:20,845,235 | G/T | — | uncertain significance |
| rs755380735 | 2:20,845,255 | T/C | — | uncertain significance |
| rs144213150 | 2:20,845,263 | C/T | — | likely benign |
| rs75352129 | 2:20,848,192 | C/T | intron variant | — |
| rs1401925896 | 2:20,850,793 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.