SLFN13
schlafen family member 13
Summary
Enables RNA endonuclease activity. Involved in rRNA catabolic process and tRNA decay. Located in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants79 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs572756318 | 17:33,765,780 | G/A | — | — |
| rs146669399 | 17:33,767,639 | T/C | — | uncertain significance |
| rs747324709 | 17:33,767,669 | T/C | — | uncertain significance |
| rs1466713734 | 17:33,767,678 | A/T | — | uncertain significance |
| rs140062622 | 17:33,767,692 | T/C | — | benign |
| rs371744448 | 17:33,767,745 | G/A | — | uncertain significance |
| rs775602714 | 17:33,767,749 | A/T | — | uncertain significance |
| rs2509004988 | 17:33,767,751 | T/C | — | uncertain significance |
| rs762882466 | 17:33,767,755 | C/G | — | uncertain significance |
| rs1265804796 | 17:33,767,777 | A/G | — | uncertain significance |
| rs1046413634 | 17:33,767,792 | C/T | — | uncertain significance |
| rs781600834 | 17:33,767,832 | G/A | — | uncertain significance |
| rs1017579933 | 17:33,767,858 | G/A | — | uncertain significance |
| rs1265247333 | 17:33,767,864 | G/T | — | uncertain significance |
| rs115182021 | 17:33,767,871 | C/T | — | uncertain significance |
| rs369932734 | 17:33,767,897 | T/C | — | uncertain significance |
| rs756915251 | 17:33,767,917 | C/G | — | uncertain significance |
| rs138317636 | 17:33,767,943 | C/T | — | uncertain significance |
| rs2509007502 | 17:33,767,991 | C/T | — | uncertain significance |
| rs773745875 | 17:33,768,038 | G/T | — | uncertain significance |
| rs1165467177 | 17:33,768,105 | C/T | — | uncertain significance |
| rs773376464 | 17:33,768,113 | C/T | — | uncertain significance |
| rs778061533 | 17:33,768,158 | G/A | — | likely benign |
| rs147476419 | 17:33,768,264 | T/C | — | likely benign |
| rs75812929 | 17:33,768,334 | T/G | — | benign |
| rs1479835367 | 17:33,768,347 | A/C | — | uncertain significance |
| rs116180460 | 17:33,768,357 | G/A | — | uncertain significance |
| rs537700636 | 17:33,768,616 | C/T | — | likely benign |
| rs556702084 | 17:33,768,618 | T/C | — | uncertain significance |
| rs778371203 | 17:33,768,643 | G/T | — | uncertain significance |
| rs2509014869 | 17:33,768,696 | G/A | — | uncertain significance |
| rs373161865 | 17:33,768,736 | G/A | — | uncertain significance |
| rs572966523 | 17:33,768,826 | C/A | — | uncertain significance |
| rs764700107 | 17:33,768,827 | G/A | — | likely benign |
| rs763731576 | 17:33,768,841 | C/T | — | uncertain significance |
| rs1173408798 | 17:33,768,892 | A/G | — | uncertain significance |
| rs768773834 | 17:33,768,909 | G/A | — | uncertain significance |
| rs1023197630 | 17:33,768,987 | C/G | — | uncertain significance |
| rs112473055 | 17:33,769,010 | T/C | — | likely benign |
| rs761522326 | 17:33,769,023 | A/G | — | uncertain significance |
| rs201693928 | 17:33,769,047 | T/C | — | uncertain significance |
| rs377103406 | 17:33,769,078 | G/A | — | uncertain significance |
| rs552965029 | 17:33,769,183 | G/A | — | likely benign |
| rs148288145 | 17:33,769,185 | A/T | — | uncertain significance |
| rs778646600 | 17:33,769,200 | G/A | — | uncertain significance |
| rs375986024 | 17:33,769,270 | G/A | — | uncertain significance |
| rs373550794 | 17:33,769,293 | T/C | — | uncertain significance |
| rs184067869 | 17:33,770,840 | T/A | — | uncertain significance |
| rs370603090 | 17:33,770,885 | C/T | — | uncertain significance |
| rs541429130 | 17:33,771,643 | C/A | — | uncertain significance |
| rs766046749 | 17:33,771,645 | T/C | — | uncertain significance |
| rs562604178 | 17:33,771,726 | G/A | — | uncertain significance |
| rs2509036733 | 17:33,771,741 | C/T | — | uncertain significance |
| rs2509036989 | 17:33,771,777 | T/C | — | uncertain significance |
| rs776590437 | 17:33,771,828 | C/G | — | likely benign |
| rs2509038230 | 17:33,771,901 | C/T | — | likely benign |
| rs150209843 | 17:33,771,943 | T/A | — | uncertain significance |
| rs2509039113 | 17:33,771,976 | C/T | — | uncertain significance |
| rs138752220 | 17:33,771,981 | G/C | — | uncertain significance |
| rs72483216 | 17:33,771,996 | A/G | — | benign |
| rs111993360 | 17:33,772,028 | T/G | — | uncertain significance |
| rs201291084 | 17:33,772,059 | A/T | — | uncertain significance |
| rs1913130306 | 17:33,772,101 | T/C | — | uncertain significance |
| rs371819305 | 17:33,772,108 | T/G | — | likely benign |
| rs752712237 | 17:33,772,144 | A/T | — | uncertain significance |
| rs758649325 | 17:33,772,150 | A/G | — | uncertain significance |
| rs944240850 | 17:33,772,168 | C/T | — | uncertain significance |
| rs150530890 | 17:33,772,233 | G/A | — | uncertain significance |
| rs115889903 | 17:33,772,246 | C/T | — | likely benign |
| rs762013186 | 17:33,772,296 | T/C | — | uncertain significance |
| rs2509044008 | 17:33,772,357 | C/T | — | uncertain significance |
| rs115892979 | 17:33,772,359 | C/T | — | uncertain significance |
| rs368869285 | 17:33,772,432 | G/C | — | uncertain significance |
| rs1567864681 | 17:33,772,521 | A/T | — | uncertain significance |
| rs114579063 | 17:33,772,551 | G/A | — | uncertain significance |
| rs1241432264 | 17:33,772,557 | C/G | — | uncertain significance |
| rs747052310 | 17:33,772,635 | C/A | — | uncertain significance |
| rs556356780 | 17:33,772,636 | C/T | — | uncertain significance |
| rs8072510 | 17:33,772,658 | G/C | stop gained | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.