Variant (rsID / SNP)
rs1055335
rs1055335 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDH19. Location: chromosome 18, position 64,176,365. The table records no clinical significance for this variant.
Reference-table entries
CDH19Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 18:64176365
- HGVS
- NM_021153.4,c.1695C>A,p.Thr565Thr
- Allele change
- Synonymous_T565T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.