Variant (rsID / SNP)

rs2459555

rs2459555 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL9A1. Location: chromosome 6, position 70,926,371. Clinical significance in the table: Benign.

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Reference-table entries

COL9A1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:70926371
Cytoband: 6q13
HGVS: NM_001851.6(COL9A1):c.*229T>C
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.