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Variant (rsID / SNP)

rs61751402

ABCA4

rs61751402 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCA4. Location: chromosome 1, position 94,495,071. Clinical significance in the table: Pathogenic.

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Reference-table entries

ABCA4Pathogenic
Clinical significance (as recorded)
Pathogenic
Variant type
single nucleotide variant
Chromosome / position
1:94495071
Cytoband
1p22.1
HGVS
NM_000350.3(ABCA4):c.4469G>A (p.Cys1490Tyr)
Allele change
Missense_C1490Y

Associated conditions / phenotypes

Severe early-childhood-onset retinal dystrophy|Retinal dystrophy|ABCA4-Related Disorders|Macular dystrophy|Retinitis pigmentosa 19|Abnormal retinal morphology

Public references

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