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Variant (rsID / SNP)

rs2855437

COL11A2

rs2855437 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL11A2. Location: chromosome 6, position 33,138,955. Clinical significance in the table: Benign.

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Reference-table entries

COL11A2Benign
Clinical significance (as recorded)
Benign
Variant type
single nucleotide variant
Chromosome / position
6:33138955
Cytoband
6p21.32
HGVS
NM_080680.3(COL11A2):c.3313-11C>T
Allele change
Silent

Associated conditions / phenotypes

Stickler Syndrome, Dominant|Fibrochondrogenesis 2|Otospondylomegaepiphyseal dysplasia, autosomal dominant|Otospondylomegaepiphyseal dysplasia, autosomal recessive|Autosomal recessive nonsyndromic hearing loss 53|Autosomal dominant nonsyndromic hearing loss 13

Public references

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