Variant (rsID / SNP)
rs234714
rs234714 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CBS. Location: chromosome 21, position 44,488,033. The table records no clinical significance for this variant.
Reference-table entries
CBSNot classified
- Variant type
- 5_prime_UTR_variant
- Chromosome / position
- 21:44488033
- HGVS
- NM_001321072.1,c.-145A>G
- Allele change
- Silent
Associated conditions / phenotypes
Heart Disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.