SLFN12L
schlafen family member 12 like
Summary
Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs55649162 | 17:33,791,668 | T/C | coding sequence variant | — |
| rs11658693 | 17:33,800,249 | A/G | downstream gene variant | — |
| rs111955358 | 17:33,801,988 | C/T | — | uncertain significance |
| rs747031939 | 17:33,802,043 | G/A | — | uncertain significance |
| rs544983067 | 17:33,802,063 | A/G | — | uncertain significance |
| rs1282869691 | 17:33,802,094 | C/G | — | uncertain significance |
| rs767784862 | 17:33,802,202 | T/G | — | uncertain significance |
| rs200292758 | 17:33,802,228 | T/C | — | uncertain significance |
| rs1040901516 | 17:33,802,272 | C/T | — | uncertain significance |
| rs747816065 | 17:33,802,273 | A/C | — | likely benign |
| rs1480128639 | 17:33,802,297 | G/A | — | uncertain significance |
| rs772380975 | 17:33,802,298 | G/C | — | uncertain significance |
| rs776868842 | 17:33,802,321 | G/T | — | uncertain significance |
| rs767306210 | 17:33,802,339 | T/C | — | uncertain significance |
| rs1913950395 | 17:33,802,371 | G/T | — | uncertain significance |
| rs2509081559 | 17:33,805,111 | A/T | — | likely benign |
| rs752176921 | 17:33,805,141 | C/T | — | uncertain significance |
| rs1161003083 | 17:33,805,189 | G/A | — | uncertain significance |
| rs1004538803 | 17:33,806,264 | G/A | — | uncertain significance |
| rs995241987 | 17:33,806,300 | A/T | — | uncertain significance |
| rs149666605 | 17:33,806,478 | C/A | — | uncertain significance |
| rs116657840 | 17:33,806,544 | T/A | — | benign |
| rs2509083274 | 17:33,806,609 | T/A | — | uncertain significance |
| rs1291052228 | 17:33,806,610 | C/T | — | uncertain significance |
| rs766672262 | 17:33,806,660 | T/G | — | uncertain significance |
| rs535994326 | 17:33,806,882 | T/A | — | uncertain significance |
| rs558500525 | 17:33,806,999 | A/G | — | uncertain significance |
| rs142712023 | 17:33,807,030 | A/T | — | benign |
| rs373139957 | 17:33,807,100 | C/G | — | uncertain significance |
| rs768815834 | 17:33,807,128 | A/G | — | uncertain significance |
| rs185307114 | 17:33,811,332 | G/A | intron variant | — |
| rs9909601 | 17:33,817,422 | A/T | coding sequence variant | — |
| rs1838149 | 17:33,819,302 | G/A | upstream gene variant | — |
| rs548491185 | 17:33,828,133 | G/T | — | — |
| rs151009319 | 17:33,835,587 | T/A | intron variant | — |
| rs8070473 | 17:33,843,512 | T/G | upstream gene variant | — |
| rs150907804 | 17:33,846,068 | G/A | upstream gene variant | — |
| rs192417831 | 17:33,849,747 | G/A | 5 prime UTR variant | — |
| rs9915940 | 17:33,856,175 | T/A | — | — |
| rs192791935 | 17:33,857,535 | A/G | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.