Variant (rsID / SNP)

rs876657718

rs876657718 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PDE6B. Location: chromosome 4, position 619,706. Clinical significance in the table: Pathogenic.

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Reference-table entries

PDE6BPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 4:619706
Cytoband: 4p16.3
HGVS: NM_000283.4(PDE6B):c.291C>A (p.Tyr97Ter)
Allele change: Nonsense_Y97X

Associated conditions / phenotypes

Retinitis pigmentosa|Retinal dystrophy

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.