SRBD1
S1 RNA binding domain 1
Summary
Predicted to enable mRNA binding activity. Predicted to be a structural constituent of ribosome. Predicted to be involved in translation. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants73 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs374414373 | 2:45,616,684 | A/G | — | uncertain significance |
| rs865875771 | 2:45,620,112 | G/C | — | uncertain significance |
| rs201615703 | 2:45,620,161 | C/G | — | uncertain significance |
| rs2466060377 | 2:45,620,206 | A/G | — | uncertain significance |
| rs200089125 | 2:45,620,239 | T/C | — | likely benign |
| rs758466471 | 2:45,620,255 | T/C | — | uncertain significance |
| rs201884615 | 2:45,640,257 | T/C | — | uncertain significance |
| rs1175529234 | 2:45,640,277 | G/A | — | uncertain significance |
| rs34959371 | 2:45,640,302 | G/C | — | likely benign |
| rs368655630 | 2:45,640,305 | T/G | — | uncertain significance |
| rs142081663 | 2:45,640,395 | C/T | — | uncertain significance |
| rs764068432 | 2:45,640,428 | G/C | — | uncertain significance |
| rs779420849 | 2:45,645,517 | G/C | — | uncertain significance |
| rs771083985 | 2:45,645,571 | G/C | — | uncertain significance |
| rs1406493564 | 2:45,645,657 | T/C | — | uncertain significance |
| rs2466132772 | 2:45,645,678 | T/C | — | uncertain significance |
| rs3213787 | 2:45,646,824 | A/G | intron variant | — |
| rs3770253 | 2:45,669,485 | C/A | — | — |
| rs17033679 | 2:45,672,633 | T/A | — | — |
| rs3770259 | 2:45,673,084 | G/A | intron variant | — |
| rs750245963 | 2:45,704,199 | C/T | — | uncertain significance |
| rs1430032098 | 2:45,704,200 | G/A | — | uncertain significance |
| rs766262381 | 2:45,704,203 | T/C | — | uncertain significance |
| rs765156998 | 2:45,715,385 | T/C | — | uncertain significance |
| rs757444637 | 2:45,715,412 | T/A | — | uncertain significance |
| rs1354567738 | 2:45,715,419 | G/C | — | uncertain significance |
| rs57288912 | 2:45,746,122 | T/C | — | — |
| rs192162433 | 2:45,749,972 | T/C | intron variant | — |
| rs899496322 | 2:45,773,871 | C/T | — | uncertain significance |
| rs761654286 | 2:45,773,946 | G/A | — | uncertain significance |
| rs773144678 | 2:45,773,960 | A/C | — | uncertain significance |
| rs61746112 | 2:45,774,694 | G/A | — | uncertain significance |
| rs372946548 | 2:45,774,746 | T/C | — | uncertain significance |
| rs145134331 | 2:45,774,748 | T/C | — | uncertain significance |
| rs191218188 | 2:45,778,270 | G/A | — | uncertain significance |
| rs753915787 | 2:45,778,414 | G/C | — | uncertain significance |
| rs778548032 | 2:45,780,796 | G/C | — | uncertain significance |
| rs768832764 | 2:45,789,829 | C/G | — | uncertain significance |
| rs745511617 | 2:45,789,868 | A/C | — | uncertain significance |
| rs72618603 | 2:45,796,171 | G/A | regulatory region variant | — |
| rs763492258 | 2:45,800,347 | T/G | — | uncertain significance |
| rs201406220 | 2:45,800,449 | G/C | — | uncertain significance |
| rs142337283 | 2:45,800,465 | C/T | — | likely benign |
| rs753662665 | 2:45,800,469 | T/G | — | uncertain significance |
| rs756306695 | 2:45,801,785 | G/C | — | uncertain significance |
| rs145942857 | 2:45,801,809 | T/C | — | uncertain significance |
| rs747001474 | 2:45,807,022 | T/C | — | uncertain significance |
| rs138516107 | 2:45,807,059 | G/C | — | uncertain significance |
| rs745779580 | 2:45,807,099 | C/A | — | uncertain significance |
| rs1295652163 | 2:45,807,143 | A/G | — | uncertain significance |
| rs768792795 | 2:45,808,840 | C/T | — | uncertain significance |
| rs761468640 | 2:45,808,870 | T/C | — | uncertain significance |
| rs144700145 | 2:45,808,923 | G/A | — | uncertain significance |
| rs2466752351 | 2:45,808,927 | T/G | — | uncertain significance |
| rs989918284 | 2:45,808,932 | A/G | — | uncertain significance |
| rs371674215 | 2:45,812,748 | G/A | — | uncertain significance |
| rs1673495008 | 2:45,812,756 | T/G | — | uncertain significance |
| rs760812902 | 2:45,826,644 | G/C | — | uncertain significance |
| rs776892185 | 2:45,826,656 | G/A | — | uncertain significance |
| rs765635909 | 2:45,826,661 | C/T | — | uncertain significance |
| rs753287117 | 2:45,826,679 | G/C | — | uncertain significance |
| rs150297990 | 2:45,826,698 | C/T | — | uncertain significance |
| rs768933365 | 2:45,826,833 | C/T | — | uncertain significance |
| rs773641981 | 2:45,826,917 | T/A | — | uncertain significance |
| rs1475409402 | 2:45,826,919 | T/C | — | uncertain significance |
| rs368355636 | 2:45,829,089 | G/T | — | uncertain significance |
| rs146680640 | 2:45,829,094 | T/C | — | uncertain significance |
| rs540155561 | 2:45,829,152 | G/A | — | uncertain significance |
| rs140742578 | 2:45,829,168 | C/G | — | uncertain significance |
| rs781549395 | 2:45,829,200 | C/T | — | uncertain significance |
| rs993372005 | 2:45,832,509 | G/T | — | uncertain significance |
| rs755375665 | 2:45,832,523 | C/T | — | uncertain significance |
| rs113207448 | 2:45,832,558 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.