| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126861547, LRIG3 (G281A +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126861547, LRIG3 (S254N +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126861547, LRIG3 (D245N +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number loss | not specified | |
| | LOC126861547, LRIG3 (D352V +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130008170, LRIG3 (G40R) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126861547, LRIG3 (E315K +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126861547, LRIG3 (D245V +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126861547, LRIG3 (F295L +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number gain | not provided | |
| | | Copy number loss | not provided | |
Click to view in NCBI Gene