R3HDM1
R3H domain containing 1
Summary
Enables RNA binding activity. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants54 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs6430580 | 2:136,321,951 | A/G | intron variant | — |
| rs56369224 | 2:136,328,890 | A/T | intron variant | — |
| rs147713032 | 2:136,351,404 | C/A | intron variant | — |
| rs775735747 | 2:136,362,501 | T/C | — | uncertain significance |
| rs6732251 | 2:136,368,563 | A/C | — | — |
| rs143470699 | 2:136,374,311 | T/G | — | uncertain significance |
| rs764869789 | 2:136,379,146 | G/A | — | uncertain significance |
| rs2467836574 | 2:136,393,486 | T/C | — | uncertain significance |
| rs1371885206 | 2:136,396,319 | G/A | — | uncertain significance |
| rs2063522411 | 2:136,396,513 | G/A | — | uncertain significance |
| rs770901687 | 2:136,396,532 | G/T | — | uncertain significance |
| rs2467859401 | 2:136,399,130 | G/C | — | uncertain significance |
| rs2467859437 | 2:136,399,138 | A/G | — | uncertain significance |
| rs755004442 | 2:136,399,180 | G/C | — | uncertain significance |
| rs748980855 | 2:136,399,217 | A/G | — | uncertain significance |
| rs2063803463 | 2:136,399,252 | G/C | — | uncertain significance |
| rs755645888 | 2:136,399,294 | T/C | — | uncertain significance |
| rs777427294 | 2:136,399,306 | C/T | — | uncertain significance |
| rs147536237 | 2:136,399,316 | C/T | — | uncertain significance |
| rs2064289760 | 2:136,403,000 | T/C | — | uncertain significance |
| rs775485367 | 2:136,403,012 | C/G | — | uncertain significance |
| rs2065177228 | 2:136,409,361 | G/A | — | uncertain significance |
| rs555940941 | 2:136,409,376 | C/G | — | uncertain significance |
| rs201789029 | 2:136,409,421 | C/G | — | uncertain significance |
| rs368537239 | 2:136,409,435 | A/G | — | uncertain significance |
| rs751840407 | 2:136,409,445 | C/T | — | uncertain significance |
| rs150498555 | 2:136,409,454 | A/G | — | uncertain significance |
| rs375588798 | 2:136,409,459 | C/G | — | uncertain significance |
| rs771600130 | 2:136,409,474 | C/A | — | uncertain significance |
| rs1435722944 | 2:136,409,594 | T/A | — | uncertain significance |
| rs2467945833 | 2:136,418,885 | C/T | — | uncertain significance |
| rs114677169 | 2:136,418,894 | C/T | — | uncertain significance |
| rs765008975 | 2:136,418,895 | G/A | — | uncertain significance |
| rs62168795 | 2:136,429,366 | T/A | — | — |
| rs760225441 | 2:136,432,938 | A/G | — | uncertain significance |
| rs1377283812 | 2:136,432,949 | G/A | — | uncertain significance |
| rs747518274 | 2:136,433,011 | G/C | — | uncertain significance |
| rs71348714 | 2:136,455,600 | G/A | intron variant | — |
| rs369352316 | 2:136,467,005 | C/G | — | uncertain significance |
| rs748749033 | 2:136,467,013 | G/A | — | uncertain significance |
| rs139565775 | 2:136,467,637 | C/A | — | uncertain significance |
| rs544498873 | 2:136,467,662 | T/C | — | uncertain significance |
| rs148125749 | 2:136,467,791 | A/G | — | likely benign |
| rs761614530 | 2:136,467,796 | G/T | — | uncertain significance |
| rs372275898 | 2:136,473,148 | T/C | — | uncertain significance |
| rs2467367206 | 2:136,473,157 | C/T | — | uncertain significance |
| rs372993003 | 2:136,473,246 | C/T | — | uncertain significance |
| rs370032006 | 2:136,473,252 | G/T | — | uncertain significance |
| rs2467396612 | 2:136,480,105 | C/T | — | uncertain significance |
| rs1575293997 | 2:136,481,524 | G/A | — | uncertain significance |
| rs962723691 | 2:136,481,609 | G/A | — | uncertain significance |
| rs116105123 | 2:136,481,683 | C/G | — | uncertain significance |
| rs190617868 | 2:136,481,785 | T/G | — | uncertain significance |
| rs141539490 | 2:136,481,819 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.