Variant (rsID / SNP)
rs3741562
rs3741562 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CERS5. Location: chromosome 12, position 50,529,736. The table records no clinical significance for this variant.
Reference-table entries
CERS5Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 12:50529736
- HGVS
- NM_001331070.3,c.753C>T,p.Asp251Asp
- Allele change
- Silent
Associated conditions / phenotypes
Silent|Synonymous_D107D|Silent|Silent|Synonymous_D251D|Synonymous_D107D
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.