Variant (rsID / SNP)

rs4659713

rs4659713 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACTN2. Location: chromosome 1, position 236,915,207. Clinical significance in the table: Benign.

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Reference-table entries

ACTN2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:236915207
Cytoband: 1q43
HGVS: NM_001103.4(ACTN2):c.1839+255G>A
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.