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Variant (rsID / SNP)

rs62646862

ABCA4

rs62646862 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCA4. Location: chromosome 1, position 94,568,686. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ABCA4Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
1:94568686
Cytoband
1p22.1
HGVS
NM_000350.3(ABCA4):c.455G>A (p.Arg152Gln)
Allele change
Missense_R152Q

Associated conditions / phenotypes

Severe early-childhood-onset retinal dystrophy|Stargardt disease|ABCA4-Related Disorders

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.