Variant (rsID / SNP)
rs3744203
rs3744203 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDR2L. Location: chromosome 17, position 73,000,061. The table records no clinical significance for this variant.
Reference-table entries
CDR2LNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:73000061
- HGVS
- NM_014603.3,c.1290A>G,p.Glu430Glu
- Allele change
- Synonymous_E430E
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.