Variant (rsID / SNP)
rs16844841
rs16844841 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LBR. Location: chromosome 1, position 225,590,675. Clinical significance in the table: Benign.
Reference-table entries
LBRBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:225590675
- Cytoband
- 1q42.12
- HGVS
- NM_002296.4(LBR):c.*330T>G
- Allele change
- Silent
Associated conditions / phenotypes
Greenberg dysplasia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.