Variant (rsID / SNP)

rs79327611

rs79327611 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC24A1. Location: chromosome 15, position 65,914,393. Clinical significance in the table: Likely benign.

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Reference-table entries

SLC24A1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 15:65914393
Cytoband: 15q22.31
HGVS: NM_004727.3(SLC24A1):c.-164C>T
Allele change: Silent

Associated conditions / phenotypes

Congenital stationary night blindness 1D

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.