| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC130009662, TNFSF11 (E27G) | Single nucleotide variant (missense variant +1 more) | Increased bone mineral density +3 more | |
| | LOC130009662, TNFSF11 (G28D) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Autosomal recessive osteopetrosis 2 +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided +2 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Autosomal recessive osteopetrosis 2 +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
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