LRRC31
leucine rich repeat containing 31
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs747415067 | 3:169,557,780 | C/T | — | uncertain significance |
| rs773226335 | 3:169,557,799 | T/G | — | uncertain significance |
| rs200600705 | 3:169,557,919 | G/A | — | uncertain significance |
| rs747923117 | 3:169,557,997 | G/A | — | likely benign |
| rs754901154 | 3:169,558,053 | A/G | — | uncertain significance |
| rs773962418 | 3:169,558,098 | G/A | — | uncertain significance |
| rs753633165 | 3:169,566,036 | T/C | — | uncertain significance |
| rs16847897 | 3:169,568,116 | G/A | — | — |
| rs2473374256 | 3:169,569,427 | C/G | — | uncertain significance |
| rs1382414425 | 3:169,569,536 | C/T | — | uncertain significance |
| rs746067420 | 3:169,569,542 | C/T | — | uncertain significance |
| rs374738133 | 3:169,569,562 | G/A | — | uncertain significance |
| rs13317603 | 3:169,570,215 | A/C | intron variant | — |
| rs532277634 | 3:169,572,614 | G/T | — | uncertain significance |
| rs374351634 | 3:169,574,244 | T/C | — | uncertain significance |
| rs762149725 | 3:169,574,524 | G/C | — | uncertain significance |
| rs202206239 | 3:169,574,540 | A/G | — | uncertain significance |
| rs2108216570 | 3:169,574,652 | A/G | — | likely benign |
| rs755427986 | 3:169,578,376 | G/C | — | uncertain significance |
| rs1260543136 | 3:169,578,388 | C/A | — | uncertain significance |
| rs1781122445 | 3:169,578,399 | A/G | — | uncertain significance |
| rs774526425 | 3:169,578,432 | G/A | — | uncertain significance |
| rs376272780 | 3:169,578,471 | G/A | — | uncertain significance |
| rs753226020 | 3:169,578,496 | G/A | — | uncertain significance |
| rs372270836 | 3:169,579,476 | C/T | — | uncertain significance |
| rs1781165868 | 3:169,579,488 | C/G | — | likely benign |
| rs1206248443 | 3:169,579,503 | C/T | — | uncertain significance |
| rs535736442 | 3:169,579,509 | A/C | — | uncertain significance |
| rs758594575 | 3:169,579,589 | C/T | — | uncertain significance |
| rs751589212 | 3:169,579,598 | T/A | — | uncertain significance |
| rs1920116 | 3:169,579,971 | G/A | intron variant | — |
| rs1333572196 | 3:169,587,498 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.