SRRM3
serine/arginine repetitive matrix 3
Summary
Predicted to enable mRNA binding activity. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants43 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs60717745 | 7:75,846,083 | C/A | — | — |
| rs535792411 | 7:75,855,082 | C/G | — | — |
| rs1554604638 | 7:75,864,450 | C/G | — | uncertain significance |
| rs781798287 | 7:75,864,485 | G/T | — | uncertain significance |
| rs1801111625 | 7:75,864,500 | T/C | — | uncertain significance |
| rs184866622 | 7:75,864,506 | C/G | — | uncertain significance |
| rs1554604700 | 7:75,864,560 | G/A | — | uncertain significance |
| rs370360717 | 7:75,877,511 | C/T | — | uncertain significance |
| rs145493761 | 7:75,881,867 | T/A | intron variant | — |
| rs1801810802 | 7:75,889,258 | G/A | — | uncertain significance |
| rs782503957 | 7:75,889,297 | G/C | — | uncertain significance |
| rs1421087459 | 7:75,889,298 | G/T | — | uncertain significance |
| rs1477837344 | 7:75,889,497 | G/A | — | uncertain significance |
| rs782117041 | 7:75,890,705 | A/C | — | uncertain significance |
| rs782446553 | 7:75,890,720 | A/T | — | uncertain significance |
| rs528273487 | 7:75,890,893 | G/A | — | uncertain significance |
| rs142979250 | 7:75,896,593 | G/A | — | likely benign |
| rs965376796 | 7:75,896,605 | G/T | — | uncertain significance |
| rs782523165 | 7:75,896,688 | G/C | — | uncertain significance |
| rs555230590 | 7:75,896,704 | G/A | — | uncertain significance |
| rs2536096606 | 7:75,896,715 | C/T | — | uncertain significance |
| rs2536096608 | 7:75,896,716 | A/T | — | uncertain significance |
| rs782489650 | 7:75,896,718 | G/T | — | uncertain significance |
| rs543973203 | 7:75,896,722 | G/C | — | uncertain significance |
| rs918990541 | 7:75,896,740 | A/C | — | uncertain significance |
| rs782486761 | 7:75,896,747 | G/T | — | likely benign |
| rs4728638 | 7:75,902,030 | C/G | — | — |
| rs142523644 | 7:75,904,098 | G/T | intron variant | — |
| rs782324462 | 7:75,910,814 | C/A | — | uncertain significance |
| rs2536116491 | 7:75,910,885 | G/C | — | uncertain significance |
| rs2536116510 | 7:75,910,895 | G/T | — | uncertain significance |
| rs1802509009 | 7:75,910,901 | G/C | — | uncertain significance |
| rs1191731971 | 7:75,910,913 | G/A | — | uncertain significance |
| rs781916490 | 7:75,910,967 | G/A | — | uncertain significance |
| rs1280134239 | 7:75,911,012 | G/C | — | uncertain significance |
| rs1337850168 | 7:75,911,047 | G/A | — | uncertain significance |
| rs2536119919 | 7:75,912,022 | C/T | — | uncertain significance |
| rs782412561 | 7:75,912,027 | G/A | — | uncertain significance |
| rs1161739203 | 7:75,912,067 | G/T | — | uncertain significance |
| rs1554612151 | 7:75,912,073 | G/A | — | uncertain significance |
| rs1438339678 | 7:75,912,080 | C/A | — | uncertain significance |
| rs781957562 | 7:75,912,160 | G/C | — | uncertain significance |
| rs781962505 | 7:75,914,933 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.