Variant (rsID / SNP)

rs28675771

rs28675771 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PDE6B. Location: chromosome 4, position 663,908. Clinical significance in the table: Benign.

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Reference-table entries

PDE6BBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 4:663908
Cytoband: 4p16.3
HGVS: NM_000283.4(PDE6B):c.*12A>G
Allele change: Silent

Associated conditions / phenotypes

Congenital stationary night blindness autosomal dominant 2|Retinitis pigmentosa|Retinitis pigmentosa 40

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.