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Variant (rsID / SNP)

rs61750155

ABCA4

rs61750155 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCA4. Location: chromosome 1, position 94,487,251. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

ABCA4Pathogenic
Clinical significance (as recorded)
Pathogenic/Likely pathogenic
Variant type
single nucleotide variant
Chromosome / position
1:94487251
Cytoband
1p22.1
HGVS
NM_000350.3(ABCA4):c.4793C>A (p.Ala1598Asp)
Allele change
Missense_A1598D

Associated conditions / phenotypes

Severe early-childhood-onset retinal dystrophy|Retinal dystrophy|Stargardt disease|Autosomal recessive retinitis pigmentosa|Retinitis pigmentosa 19

Public references

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