Variant (rsID / SNP)

rs192448853

rs192448853 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CNGB3. Location: chromosome 8, position 87,590,934. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

CNGB3Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 8:87590934
Cytoband: 8q21.3
HGVS: NM_019098.5(CNGB3):c.2086C>T (p.Arg696Ter)
Allele change: Nonsense_R696X

Associated conditions / phenotypes

Achromatopsia 3

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.