Variant (rsID / SNP)

rs146170855

rs146170855 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CNGB1. Location: chromosome 16, position 57,984,441. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

CNGB1Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 16:57984441
Cytoband: 16q21
HGVS: NM_001297.5(CNGB1):c.878G>A (p.Ser293Asn)
Allele change: Missense_S287N

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.