Variant (rsID / SNP)

rs915201

rs915201 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCA4. Location: chromosome 1, position 94,481,596. Clinical significance in the table: Benign.

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Reference-table entries

ABCA4Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:94481596
Cytoband: 1p22.1
HGVS: NM_000350.3(ABCA4):c.5197-186T>C
Allele change: Silent

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.