Variant (rsID / SNP)
rs2306862
rs2306862 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRP5. Location: chromosome 11, position 68,177,510. Clinical significance in the table: Benign.
Reference-table entries
LRP5Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:68177510
- Cytoband
- 11q13.2
- HGVS
- NM_002335.4(LRP5):c.2220C>T (p.Asn740=)
- Allele change
- Synonymous_N740N
Associated conditions / phenotypes
Bone mineral density quantitative trait locus 1|Osteogenesis imperfecta|Increased bone mineral density
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.