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Variant (rsID / SNP)

rs148685646

LRP5

rs148685646 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRP5. Location: chromosome 11, position 68,201,315. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

LRP5Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
11:68201315
Cytoband
11q13.2
HGVS
NM_002335.4(LRP5):c.4000+9C>T
Allele change
Silent

Associated conditions / phenotypes

Postmenopausal osteoporosis|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.