Variant (rsID / SNP)
rs1127065
rs1127065 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CAMK2B. Location: chromosome 7, position 44,259,871. The table records no clinical significance for this variant.
Reference-table entries
CAMK2BNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 7:44259871
- HGVS
- NM_001220.5,c.1791G>A,p.Pro597Pro
- Allele change
- Synonymous_P410P
Associated conditions / phenotypes
Synonymous_P597P|Synonymous_P473P|Synonymous_P473P|Synonymous_P380P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.