Variant (rsID / SNP)

rs201054854

rs201054854 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL9A2. Location: chromosome 1, position 40,770,175. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

COL9A2Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 1:40770175
Cytoband: 1p34.2
HGVS: NM_001852.4(COL9A2):c.1188G>A (p.Val396=)
Allele change: Synonymous_V396V

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.