Variant (rsID / SNP)

rs55941599

rs55941599 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RHO. Location: chromosome 3, position 129,252,874. Clinical significance in the table: Benign.

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Reference-table entries

RHOBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:129252874
Cytoband: 3q22.1
HGVS: NM_000539.3(RHO):c.*313C>T
Allele change: Silent

Associated conditions / phenotypes

Retinitis pigmentosa|Congenital stationary night blindness autosomal dominant 1

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.