Variant (rsID / SNP)
rs11542227
rs11542227 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CAMK2B. Location: chromosome 7, position 44,282,877. The table records no clinical significance for this variant.
Reference-table entries
CAMK2BNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 7:44282877
- HGVS
- NM_001220.5,c.573T>C,p.Tyr191Tyr
- Allele change
- Synonymous_Y191Y
Associated conditions / phenotypes
Synonymous_Y191Y|Synonymous_Y191Y|Synonymous_Y191Y|Synonymous_Y191Y
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.