Variant (rsID / SNP)

rs35571449

rs35571449 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC24A1. Location: chromosome 15, position 65,917,355. Clinical significance in the table: Benign.

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Reference-table entries

SLC24A1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 15:65917355
Cytoband: 15q22.31
HGVS: NM_004727.3(SLC24A1):c.937T>G (p.Leu313Val)
Allele change: Missense_L313V

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.