| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | LOC130059892, SERPINF1 (S81C) | Single nucleotide variant (missense variant +1 more) | Osteogenesis imperfecta type 6 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Osteogenesis imperfecta type 6 +2 more | |
Click to view in NCBI Gene