LRRC74A
leucine rich repeat containing 74A
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1248930953 | 14:77,292,848 | C/G | — | uncertain significance |
| rs374629334 | 14:77,292,911 | C/T | — | uncertain significance |
| rs762701243 | 14:77,294,693 | G/A | — | uncertain significance |
| rs1174509003 | 14:77,294,733 | A/G | — | uncertain significance |
| rs1895954590 | 14:77,297,647 | G/A | — | uncertain significance |
| rs557701075 | 14:77,297,654 | A/G | — | uncertain significance |
| rs748570959 | 14:77,297,674 | G/A | — | uncertain significance |
| rs149051733 | 14:77,297,688 | G/C | — | uncertain significance |
| rs143093578 | 14:77,297,690 | G/A | — | uncertain significance |
| rs779853435 | 14:77,302,638 | A/C | — | uncertain significance |
| rs370337650 | 14:77,304,245 | G/A | — | uncertain significance |
| rs201346482 | 14:77,304,301 | C/A | — | uncertain significance |
| rs577287444 | 14:77,310,071 | G/C | — | — |
| rs1278712896 | 14:77,318,725 | A/G | — | uncertain significance |
| rs138170515 | 14:77,318,726 | C/T | — | uncertain significance |
| rs202130671 | 14:77,319,566 | T/G | — | uncertain significance |
| rs371108341 | 14:77,319,575 | C/G | — | uncertain significance |
| rs558316728 | 14:77,319,641 | G/T | — | uncertain significance |
| rs779195574 | 14:77,319,650 | G/A | — | uncertain significance |
| rs574874334 | 14:77,319,658 | G/T | — | uncertain significance |
| rs1421605472 | 14:77,319,659 | T/C | — | likely benign |
| rs764059406 | 14:77,319,673 | G/A | — | likely benign |
| rs7146257 | 14:77,319,693 | T/C | — | benign |
| rs755479933 | 14:77,319,745 | G/A | — | uncertain significance |
| rs575564526 | 14:77,327,039 | G/A | — | uncertain significance |
| rs187527026 | 14:77,327,051 | G/A | — | uncertain significance |
| rs746898980 | 14:77,327,105 | G/C | — | uncertain significance |
| rs745642878 | 14:77,327,106 | T/A | — | uncertain significance |
| rs367749455 | 14:77,327,126 | G/C | — | uncertain significance |
| rs2503358785 | 14:77,327,138 | A/G | — | uncertain significance |
| rs140195914 | 14:77,332,301 | C/T | — | benign |
| rs2503380125 | 14:77,332,411 | T/C | — | uncertain significance |
| rs780438068 | 14:77,333,751 | T/A | — | uncertain significance |
| rs370995005 | 14:77,333,753 | G/A | — | uncertain significance |
| rs200364336 | 14:77,333,756 | G/C | — | uncertain significance |
| rs2503394501 | 14:77,333,777 | T/A | — | uncertain significance |
| rs144379825 | 14:77,336,461 | G/T | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.