Variant (rsID / SNP)
rs1801197
rs1801197 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CALCR. Location: chromosome 7, position 93,055,753. Clinical significance in the table: Benign.
Reference-table entries
CALCRBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:93055753
- Cytoband
- 7q21.3
- HGVS
- NM_001742.4(CALCR):c.1340T>C (p.Leu447Pro)
- Allele change
- Missense_L447P
Associated conditions / phenotypes
Bone mineral density quantitative trait locus 15
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.