R3HDM2
R3H domain containing 2
Summary
Enables RNA binding activity. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants55 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs142251653 | 12:57,648,623 | C/T | — | uncertain significance |
| rs749885285 | 12:57,648,716 | G/A | — | uncertain significance |
| rs777878496 | 12:57,648,756 | C/A | — | uncertain significance |
| rs1461581018 | 12:57,648,773 | C/A | — | uncertain significance |
| rs1188128428 | 12:57,648,799 | C/G | — | uncertain significance |
| rs746487037 | 12:57,650,207 | G/A | — | uncertain significance |
| rs865863968 | 12:57,650,229 | G/A | — | uncertain significance |
| rs1232209458 | 12:57,650,265 | G/A | — | uncertain significance |
| rs772025551 | 12:57,651,806 | T/A | — | uncertain significance |
| rs372700229 | 12:57,652,735 | A/G | — | uncertain significance |
| rs146780443 | 12:57,660,572 | G/A | — | benign |
| rs751239330 | 12:57,662,108 | G/C | — | uncertain significance |
| rs2043049521 | 12:57,662,799 | G/A | — | uncertain significance |
| rs758514414 | 12:57,662,800 | G/C | — | uncertain significance |
| rs1438737313 | 12:57,662,842 | G/T | — | uncertain significance |
| rs778397922 | 12:57,662,854 | T/A | — | uncertain significance |
| rs762584623 | 12:57,663,177 | C/T | — | uncertain significance |
| rs755622952 | 12:57,663,760 | G/T | — | uncertain significance |
| rs778634125 | 12:57,663,777 | C/G | — | uncertain significance |
| rs202044319 | 12:57,674,184 | G/A | — | uncertain significance |
| rs759991344 | 12:57,674,203 | G/A | — | uncertain significance |
| rs754924568 | 12:57,674,257 | G/A | — | uncertain significance |
| rs750868851 | 12:57,677,652 | T/A | — | uncertain significance |
| rs767351635 | 12:57,677,712 | G/T | — | uncertain significance |
| rs1241975207 | 12:57,677,835 | T/A | — | uncertain significance |
| rs56205943 | 12:57,679,414 | G/A | intron variant | — |
| rs2548587772 | 12:57,682,662 | G/A | — | uncertain significance |
| rs951014365 | 12:57,689,236 | T/A | — | uncertain significance |
| rs12313762 | 12:57,692,470 | C/G | — | — |
| rs557260090 | 12:57,706,653 | G/A | — | — |
| rs28473132 | 12:57,707,358 | A/T | intron variant | — |
| rs7484541 | 12:57,714,803 | A/T | intron variant | — |
| rs186767801 | 12:57,727,682 | G/A | intron variant | — |
| rs7397189 | 12:57,728,776 | T/G | intron variant | — |
| rs79395356 | 12:57,738,600 | T/G | intron variant | — |
| rs6581138 | 12:57,744,864 | G/A | intron variant | — |
| rs12313306 | 12:57,751,854 | C/T | intron variant | — |
| rs537596349 | 12:57,753,833 | T/A | — | — |
| rs555730055 | 12:57,753,835 | T/C | — | — |
| rs34537746 | 12:57,755,151 | T/A | — | — |
| rs11172181 | 12:57,756,005 | T/C | intron variant | — |
| rs11172185 | 12:57,764,183 | G/T | — | — |
| rs4760254 | 12:57,766,392 | G/C | regulatory region variant | — |
| rs7971133 | 12:57,770,098 | C/T | intron variant | — |
| rs12315434 | 12:57,780,936 | A/C | regulatory region variant | — |
| rs2122982 | 12:57,781,893 | G/A | intron variant | — |
| rs68147365 | 12:57,789,359 | G/T | — | — |
| rs572198 | 12:57,791,986 | C/T | intron variant | — |
| rs113742467 | 12:57,792,513 | C/T | — | — |
| rs11613352 | 12:57,792,580 | C/T | intron variant | — |
| rs11172205 | 12:57,806,846 | G/T | upstream gene variant | — |
| rs1106766 | 12:57,809,456 | C/T | downstream gene variant | — |
| rs55772485 | 12:57,821,082 | T/A | upstream gene variant | — |
| rs7964492 | 12:57,823,585 | A/C | regulatory region variant | — |
| rs183384649 | 12:57,823,971 | G/A | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.