Variant (rsID / SNP)

rs9289713

rs9289713 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLOD2. Location: chromosome 3, position 145,824,025. Clinical significance in the table: Benign.

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Reference-table entries

PLOD2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:145824025
Cytoband: 3q24
HGVS: NM_182943.3(PLOD2):c.615+294A>G
Allele change: Silent

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.