Variant (rsID / SNP)
rs4681297
rs4681297 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLOD2. Location: chromosome 3, position 145,838,895. Clinical significance in the table: Benign.
Reference-table entries
PLOD2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:145838895
- Cytoband
- 3q24
- HGVS
- NM_182943.3(PLOD2):c.338+4G>A
- Allele change
- Silent
Associated conditions / phenotypes
Bruck syndrome 2
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.