Variant (rsID / SNP)
rs4541465
rs4541465 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APELA. Location: chromosome 4, position 165,800,154. Clinical significance in the table: Likely_benign.
Reference-table entries
APELALikely benign
- Clinical significance (as recorded)
- Likely_benign
- Variant type
- synonymous_variant
- Chromosome / position
- 4:165800154
- HGVS
- NM_001297550.2,c.159T>C,p.Phe53Phe
- Allele change
- Synonymous_F53F
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.