Variant (rsID / SNP)
rs12964819
rs12964819 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDH20. Location: chromosome 18, position 59,166,541. The table records no clinical significance for this variant.
Reference-table entries
CDH20Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 18:59166541
- HGVS
- NM_031891.4,c.369C>T,p.Asp123Asp
- Allele change
- Synonymous_D123D
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.