LRRC43
leucine rich repeat containing 43
Known Variants43 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs772485109 | 12:122,653,620 | C/T | — | — |
| rs11608363 | 12:122,659,785 | C/G | — | — |
| rs6489188 | 12:122,660,776 | T/G | — | — |
| rs7953139 | 12:122,662,541 | T/C | upstream gene variant | — |
| rs764380514 | 12:122,667,696 | A/T | — | uncertain significance |
| rs1475313553 | 12:122,667,716 | T/A | — | uncertain significance |
| rs577217667 | 12:122,667,732 | A/G | — | uncertain significance |
| rs890083607 | 12:122,667,738 | G/T | — | uncertain significance |
| rs1007220417 | 12:122,667,755 | C/T | — | uncertain significance |
| rs775440236 | 12:122,667,800 | A/C | — | likely benign |
| rs1953601884 | 12:122,667,818 | T/C | — | uncertain significance |
| rs10847623 | 12:122,668,965 | T/A | — | — |
| rs959330706 | 12:122,669,081 | C/A | — | uncertain significance |
| rs200229491 | 12:122,669,096 | C/T | — | uncertain significance |
| rs750177453 | 12:122,669,144 | G/T | — | uncertain significance |
| rs767042268 | 12:122,669,217 | C/T | — | uncertain significance |
| rs372375067 | 12:122,669,255 | C/T | — | uncertain significance |
| rs1593144808 | 12:122,669,262 | C/T | — | uncertain significance |
| rs746323946 | 12:122,669,268 | C/T | — | likely benign |
| rs199554806 | 12:122,669,310 | G/C | — | uncertain significance |
| rs4758678 | 12:122,671,355 | G/C | — | — |
| rs377167993 | 12:122,674,699 | C/G | — | uncertain significance |
| rs199533998 | 12:122,674,739 | C/T | — | uncertain significance |
| rs558151255 | 12:122,674,742 | G/C | — | uncertain significance |
| rs533359635 | 12:122,674,810 | T/G | — | uncertain significance |
| rs767637298 | 12:122,674,849 | G/A | — | uncertain significance |
| rs201401336 | 12:122,674,867 | G/A | — | uncertain significance |
| rs952812974 | 12:122,674,904 | G/T | — | uncertain significance |
| rs778932116 | 12:122,676,097 | G/A | — | likely benign |
| rs751519017 | 12:122,677,358 | G/A | — | uncertain significance |
| rs201841622 | 12:122,677,385 | A/G | — | uncertain significance |
| rs200517782 | 12:122,677,423 | G/C | — | uncertain significance |
| rs773915313 | 12:122,677,521 | G/A | — | uncertain significance |
| rs1225478348 | 12:122,684,812 | A/G | — | uncertain significance |
| rs1355282722 | 12:122,684,861 | C/A | — | uncertain significance |
| rs199768950 | 12:122,685,401 | G/A | — | uncertain significance |
| rs1165796150 | 12:122,685,434 | T/A | — | uncertain significance |
| rs766071496 | 12:122,685,437 | G/A | — | uncertain significance |
| rs767582329 | 12:122,685,443 | G/T | — | uncertain significance |
| rs758327800 | 12:122,685,446 | C/T | — | uncertain significance |
| rs1953866997 | 12:122,687,912 | C/T | — | uncertain significance |
| rs748869203 | 12:122,687,931 | A/G | — | uncertain significance |
| rs765493608 | 12:122,687,965 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.