Variant (rsID / SNP)
rs198444
rs198444 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DAGLA. Location: chromosome 11, position 61,505,168. The table records no clinical significance for this variant.
Reference-table entries
DAGLANot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 11:61505168
- HGVS
- NM_006133.3,c.1524G>A,p.Ala508Ala
- Allele change
- Synonymous_A508A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.