FBRSL1
fibrosin like 1
Summary
Enables RNA binding activity. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants163 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs949454511 | 12:133,067,202 | G/A | — | uncertain significance |
| rs1353622759 | 12:133,067,236 | C/T | — | uncertain significance |
| rs1016361246 | 12:133,067,250 | C/T | — | uncertain significance |
| rs2541447147 | 12:133,067,271 | G/T | — | likely benign |
| rs1194276361 | 12:133,067,275 | C/T | — | uncertain significance |
| rs1235267606 | 12:133,067,314 | C/A | — | uncertain significance |
| rs2030704811 | 12:133,067,317 | C/G | — | uncertain significance |
| rs1426715637 | 12:133,067,325 | G/A | — | uncertain significance |
| rs772630698 | 12:133,067,328 | G/A | — | uncertain significance |
| rs555665082 | 12:133,067,368 | G/A | — | uncertain significance |
| rs12811407 | 12:133,069,698 | G/A | regulatory region variant | — |
| rs36098511 | 12:133,080,449 | A/T | intron variant | — |
| rs1039795231 | 12:133,084,784 | C/T | — | uncertain significance |
| rs1271488662 | 12:133,084,805 | C/G | — | uncertain significance |
| rs544044707 | 12:133,084,824 | C/T | — | uncertain significance |
| rs377213746 | 12:133,084,826 | C/G | — | uncertain significance |
| rs2541118501 | 12:133,084,877 | C/T | — | uncertain significance |
| rs2033928427 | 12:133,084,893 | C/T | — | uncertain significance |
| rs764604501 | 12:133,084,905 | C/T | — | uncertain significance |
| rs2033932444 | 12:133,084,935 | A/G | — | uncertain significance |
| rs1003362591 | 12:133,086,075 | C/T | — | likely benign |
| rs555389753 | 12:133,086,735 | G/A | — | likely benign |
| rs2541149623 | 12:133,086,978 | A/G | — | likely benign |
| rs3751297 | 12:133,088,165 | G/A | intron variant | — |
| rs201533476 | 12:133,102,332 | G/A | — | uncertain significance |
| rs1160067316 | 12:133,102,344 | G/A | — | uncertain significance |
| rs775636928 | 12:133,102,347 | G/A | — | uncertain significance |
| rs186991682 | 12:133,102,351 | G/A | — | uncertain significance |
| rs750809377 | 12:133,102,393 | G/A | — | likely benign |
| rs756508813 | 12:133,102,399 | C/T | — | uncertain significance |
| rs4883565 | 12:133,104,735 | T/C | intron variant | — |
| rs75680255 | 12:133,126,495 | G/A | regulatory region variant | — |
| rs10781620 | 12:133,138,557 | A/T | — | — |
| rs111605474 | 12:133,139,597 | A/C | — | — |
| rs78644250 | 12:133,140,329 | C/G | intron variant | — |
| rs111599055 | 12:133,140,361 | A/C | intron variant | — |
| rs4992759 | 12:133,140,409 | T/C | intron variant | — |
| rs4992758 | 12:133,140,410 | G/C | intron variant | — |
| rs5023078 | 12:133,142,118 | T/C | — | — |
| rs997589705 | 12:133,144,106 | G/A | — | uncertain significance |
| rs1203677751 | 12:133,146,525 | G/C | — | uncertain significance |
| rs1480411952 | 12:133,146,541 | G/T | — | uncertain significance |
| rs1385360353 | 12:133,146,556 | A/C | — | uncertain significance |
| rs763455650 | 12:133,146,581 | G/A | — | conflicting classifications of pathogenicity |
| rs1332964594 | 12:133,146,583 | G/A | — | uncertain significance |
| rs1354727796 | 12:133,146,592 | G/A | — | likely benign |
| rs562553564 | 12:133,146,595 | G/A | — | uncertain significance |
| rs767758496 | 12:133,146,623 | C/T | — | uncertain significance |
| rs1041928176 | 12:133,146,634 | G/A | — | uncertain significance |
| rs531199362 | 12:133,146,635 | C/T | — | uncertain significance |
| rs756438425 | 12:133,146,646 | G/A | — | uncertain significance |
| rs953732736 | 12:133,146,653 | C/T | — | uncertain significance |
| rs752450409 | 12:133,146,658 | G/A | — | uncertain significance |
| rs180891480 | 12:133,146,665 | G/A | — | likely benign |
| rs918463518 | 12:133,146,670 | A/G | — | conflicting classifications of pathogenicity |
| rs903746056 | 12:133,146,691 | C/A | — | uncertain significance |
| rs566934494 | 12:133,146,696 | C/T | — | likely benign |
| rs937394316 | 12:133,146,707 | G/A | — | uncertain significance |
| rs963013936 | 12:133,146,712 | A/G | — | uncertain significance |
| rs569313226 | 12:133,146,722 | C/T | — | uncertain significance |
| rs1259404904 | 12:133,146,736 | C/T | — | uncertain significance |
| rs554905966 | 12:133,146,739 | C/T | — | uncertain significance |
| rs1467287441 | 12:133,146,742 | G/A | — | uncertain significance |
| rs965411150 | 12:133,146,778 | G/A | — | uncertain significance |
| rs983981809 | 12:133,146,786 | G/A | — | likely benign |
| rs2039912821 | 12:133,146,787 | G/A | — | uncertain significance |
| rs2541424877 | 12:133,146,967 | T/C | — | uncertain significance |
| rs775516121 | 12:133,147,016 | G/A | — | uncertain significance |
| rs1341093919 | 12:133,147,042 | G/A | — | uncertain significance |
| rs888111081 | 12:133,147,072 | C/T | — | uncertain significance |
| rs1401471128 | 12:133,147,766 | G/A | — | likely benign |
| rs1006487953 | 12:133,147,898 | G/A | — | uncertain significance |
| rs895336919 | 12:133,147,925 | C/T | — | uncertain significance |
| rs368308315 | 12:133,147,971 | C/T | — | uncertain significance |
| rs1301458865 | 12:133,147,989 | C/A | — | uncertain significance |
| rs965346395 | 12:133,148,085 | C/T | — | uncertain significance |
| rs745951720 | 12:133,148,106 | C/T | — | uncertain significance |
| rs555033677 | 12:133,148,109 | C/T | — | uncertain significance |
| rs746418990 | 12:133,148,914 | G/A | — | uncertain significance |
| rs369215284 | 12:133,149,153 | C/A | — | uncertain significance |
| rs201936807 | 12:133,149,179 | G/A | — | uncertain significance |
| rs2040109939 | 12:133,149,200 | C/G | — | likely pathogenic |
| rs781066357 | 12:133,150,920 | C/T | — | uncertain significance |
| rs745652513 | 12:133,150,921 | G/A | — | uncertain significance |
| rs941267853 | 12:133,150,957 | C/T | — | likely benign |
| rs546771681 | 12:133,150,984 | C/T | — | uncertain significance |
| rs376038505 | 12:133,151,005 | G/A | — | uncertain significance |
| rs376282005 | 12:133,151,061 | G/A | — | uncertain significance |
| rs370695435 | 12:133,151,105 | C/T | — | likely benign |
| rs371732785 | 12:133,151,130 | C/T | — | uncertain significance |
| rs1218766612 | 12:133,153,386 | A/C | — | uncertain significance |
| rs775060512 | 12:133,153,392 | A/G | — | uncertain significance |
| rs979511863 | 12:133,153,452 | C/T | — | uncertain significance |
| rs537019983 | 12:133,153,460 | G/A | — | uncertain significance |
| rs2040416025 | 12:133,153,485 | A/G | — | uncertain significance |
| rs75471611 | 12:133,155,312 | C/G | — | — |
| rs1328722895 | 12:133,158,045 | A/G | — | uncertain significance |
| rs1274787495 | 12:133,158,076 | G/C | — | uncertain significance |
| rs1420336153 | 12:133,158,103 | G/A | — | uncertain significance |
| rs749751607 | 12:133,158,105 | G/T | — | likely benign |
Showing 100 of 163 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.