Variant (rsID / SNP)

rs121912885

rs121912885 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL2A1. Location: chromosome 12, position 48,377,218. Clinical significance in the table: Pathogenic.

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Reference-table entries

COL2A1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 12:48377218
Cytoband: 12q13.11
HGVS: NM_001844.5(COL2A1):c.1999C>T (p.Leu667Phe)
Allele change: Missense_L667F

Associated conditions / phenotypes

Stickler syndrome, type I, nonsyndromic ocular|Stickler syndrome type 1

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.