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Variant (rsID / SNP)

rs182445749

PDE6C

rs182445749 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PDE6C. Location: chromosome 10, position 95,415,508. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

PDE6CBenign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
10:95415508
Cytoband
10q23.33
HGVS
NM_006204.4(PDE6C):c.1936-9A>G
Allele change
Silent

Associated conditions / phenotypes

Cone dystrophy 4|Achromatopsia

Public references

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