RTL9
retrotransposon Gag like 9
Known Variants78 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs10521528 | X:109,689,152 | A/G | intron variant | — |
| rs67648651 | X:109,693,274 | T/C | regulatory region variant | — |
| rs759928039 | X:109,693,928 | T/C | — | uncertain significance |
| rs150383653 | X:109,693,965 | G/C | — | uncertain significance |
| rs377448143 | X:109,694,165 | C/T | — | uncertain significance |
| rs759740444 | X:109,694,437 | C/G | — | uncertain significance |
| rs144726953 | X:109,694,468 | T/C | — | conflicting classifications of pathogenicity |
| rs911288716 | X:109,694,733 | C/G | — | likely benign |
| rs766385379 | X:109,694,759 | G/A | — | uncertain significance |
| rs199759157 | X:109,694,771 | C/T | — | uncertain significance |
| rs140162353 | X:109,694,813 | C/T | — | uncertain significance |
| rs781739124 | X:109,694,825 | T/C | — | uncertain significance |
| rs751310287 | X:109,694,844 | G/A | — | uncertain significance |
| rs780040795 | X:109,694,855 | C/G | — | uncertain significance |
| rs749364881 | X:109,694,863 | G/T | — | uncertain significance |
| rs774410408 | X:109,694,879 | C/A | — | uncertain significance |
| rs775201044 | X:109,694,932 | A/T | — | uncertain significance |
| rs1005978898 | X:109,694,992 | G/C | — | likely benign |
| rs188623114 | X:109,695,008 | C/T | — | likely benign |
| rs2068943219 | X:109,695,031 | G/A | — | uncertain significance |
| rs2522935081 | X:109,695,071 | G/C | — | uncertain significance |
| rs138209810 | X:109,695,086 | C/T | — | uncertain significance |
| rs766678813 | X:109,695,139 | C/T | — | uncertain significance |
| rs765708019 | X:109,695,295 | G/A | — | uncertain significance |
| rs776026057 | X:109,695,314 | G/C | — | uncertain significance |
| rs898648421 | X:109,695,323 | C/A | — | uncertain significance |
| rs150857628 | X:109,695,375 | G/A | — | uncertain significance |
| rs752578391 | X:109,695,385 | C/T | — | uncertain significance |
| rs769283529 | X:109,695,428 | T/C | — | uncertain significance |
| rs759267458 | X:109,695,465 | A/C | — | uncertain significance |
| rs1165474949 | X:109,695,486 | A/C | — | uncertain significance |
| rs769220003 | X:109,695,487 | G/A | — | uncertain significance |
| rs1276037481 | X:109,695,491 | T/C | — | uncertain significance |
| rs2068947862 | X:109,695,492 | G/A | — | uncertain significance |
| rs2522937394 | X:109,695,589 | G/A | — | uncertain significance |
| rs146389599 | X:109,695,755 | C/T | — | uncertain significance |
| rs1205299045 | X:109,695,797 | G/A | — | uncertain significance |
| rs773492564 | X:109,695,961 | C/T | — | uncertain significance |
| rs760284501 | X:109,695,979 | G/A | — | uncertain significance |
| rs151173460 | X:109,695,998 | T/C | — | conflicting classifications of pathogenicity |
| rs764969366 | X:109,696,000 | C/T | — | uncertain significance |
| rs1407663652 | X:109,696,043 | T/C | — | likely benign |
| rs1440759499 | X:109,696,114 | C/G | — | uncertain significance |
| rs1326842119 | X:109,696,147 | T/C | — | uncertain significance |
| rs750897143 | X:109,696,161 | G/A | — | uncertain significance |
| rs138630207 | X:109,696,280 | C/T | — | uncertain significance |
| rs763792910 | X:109,696,282 | C/G | — | uncertain significance |
| rs768040774 | X:109,696,291 | G/A | — | uncertain significance |
| rs2522941600 | X:109,696,324 | G/A | — | uncertain significance |
| rs1445476645 | X:109,696,348 | C/T | — | uncertain significance |
| rs1038150898 | X:109,696,361 | C/T | — | uncertain significance |
| rs146088998 | X:109,696,543 | C/T | — | uncertain significance |
| rs752820274 | X:109,696,649 | A/G | — | uncertain significance |
| rs375048237 | X:109,696,655 | C/A | — | uncertain significance |
| rs745784735 | X:109,696,715 | C/T | — | uncertain significance |
| rs775761617 | X:109,696,730 | T/C | — | uncertain significance |
| rs911607106 | X:109,696,774 | A/G | — | uncertain significance |
| rs754963980 | X:109,696,787 | A/G | — | uncertain significance |
| rs144417719 | X:109,696,841 | G/T | — | uncertain significance |
| rs776104816 | X:109,696,861 | A/G | — | uncertain significance |
| rs749404863 | X:109,696,862 | C/A | — | uncertain significance |
| rs768801251 | X:109,696,865 | C/T | — | uncertain significance |
| rs2522944684 | X:109,696,868 | A/G | — | uncertain significance |
| rs148401387 | X:109,696,873 | G/A | — | uncertain significance |
| rs375557311 | X:109,696,875 | G/C | — | likely benign |
| rs145170816 | X:109,696,883 | G/A | — | uncertain significance |
| rs190170443 | X:109,696,895 | C/T | — | uncertain significance |
| rs1163071757 | X:109,696,904 | G/A | — | uncertain significance |
| rs2522945723 | X:109,697,057 | C/T | — | likely benign |
| rs771130284 | X:109,697,207 | C/T | — | uncertain significance |
| rs1271585694 | X:109,697,225 | C/T | — | uncertain significance |
| rs772118985 | X:109,697,376 | G/T | — | uncertain significance |
| rs41306249 | X:109,697,443 | T/C | missense variant | — |
| rs142031687 | X:109,697,800 | G/C | — | uncertain significance |
| rs1336899261 | X:109,697,830 | T/C | — | uncertain significance |
| rs896624507 | X:109,697,843 | A/C | — | uncertain significance |
| rs1283214166 | X:109,698,479 | C/T | — | uncertain significance |
| rs2522951869 | X:109,698,542 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.