Variant (rsID / SNP)

rs3737821

rs3737821 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL9A2. Location: chromosome 1, position 40,768,344. Clinical significance in the table: Benign.

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Reference-table entries

COL9A2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:40768344
Cytoband: 1p34.2
HGVS: NM_001852.4(COL9A2):c.1741G>A (p.Val581Ile)
Allele change: Missense_V581I

Associated conditions / phenotypes

Epiphyseal dysplasia, multiple, 2

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.