Variant (rsID / SNP)

rs1056392

rs1056392 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OPA1. Location: chromosome 3, position 193,414,733. Clinical significance in the table: Benign.

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Reference-table entries

OPA1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:193414733
Cytoband: 3q29
HGVS: NM_130837.3(OPA1):c.*2344A>G
Allele change: Silent

Associated conditions / phenotypes

Autosomal dominant optic atrophy classic form

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.