Variant (rsID / SNP)
rs1208984
rs1208984 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLOD1. Location: chromosome 1, position 11,995,176. Clinical significance in the table: Benign.
Reference-table entries
PLOD1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:11995176
- Cytoband
- 1p36.22
- HGVS
- NM_000302.4(PLOD1):c.76+264A>G
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.