Variant (rsID / SNP)
rs2073618
rs2073618 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TNFRSF11B. Location: chromosome 8, position 119,964,052. Clinical significance in the table: Benign.
Reference-table entries
TNFRSF11BBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 8:119964052
- Cytoband
- 8q24.12
- HGVS
- NM_002546.4(TNFRSF11B):c.9C>G (p.Asn3Lys)
- Allele change
- Missense_N3K
Associated conditions / phenotypes
Hyperphosphatasemia with bone disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.