Variant (rsID / SNP)
rs6451993
rs6451993 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDH12. Location: chromosome 5, position 21,752,056. The table records no clinical significance for this variant.
Reference-table entries
CDH12Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 5:21752056
- HGVS
- NM_001317227.2,c.2175T>C,p.Asp725Asp
- Allele change
- Synonymous_D725D
Associated conditions / phenotypes
Synonymous_D725D|Synonymous_D685D|Synonymous_D501D|Synonymous_D725D
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.