Variant (rsID / SNP)
rs2289272
rs2289272 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATP2B2. Location: chromosome 3, position 10,413,526. Clinical significance in the table: Benign.
Reference-table entries
ATP2B2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- synonymous_variant
- Chromosome / position
- 3:10413526
- HGVS
- NM_001001331.4,c.1626C>T,p.Ile542Ile
- Allele change
- Synonymous_I497I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.