Variant (rsID / SNP)

rs11078563

rs11078563 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRPF8. Location: chromosome 17, position 1,576,369. Clinical significance in the table: Benign.

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Reference-table entries

PRPF8Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:1576369
Cytoband: 17p13.3
HGVS: NM_006445.4(PRPF8):c.3774+6G>A
Allele change: Silent

Associated conditions / phenotypes

Retinitis pigmentosa

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.