Variant (rsID / SNP)
rs3738544
rs3738544 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACTN2. Location: chromosome 1, position 236,914,576. Clinical significance in the table: Benign.
Reference-table entries
ACTN2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:236914576
- Cytoband
- 1q43
- HGVS
- NM_001103.4(ACTN2):c.1657-194C>T
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.