Variant (rsID / SNP)
rs513043
rs513043 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LMNA. Location: chromosome 1, position 156,099,669. Clinical significance in the table: Benign.
Reference-table entries
LMNABenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:156099669
- Cytoband
- 1q22
- HGVS
- NM_170707.4(LMNA):c.357-739T>G
- Allele change
- Silent
Associated conditions / phenotypes
Hutchinson-Gilford syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.