Variant (rsID / SNP)
rs6142884
rs6142884 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDH4. Location: chromosome 20, position 60,503,350. The table records no clinical significance for this variant.
Reference-table entries
CDH4Not classified
- Variant type
- missense_variant
- Chromosome / position
- 20:60503350
- HGVS
- NM_001794.5,c.1874A>G,p.Lys625Arg
- Allele change
- Missense_K625R
Associated conditions / phenotypes
Chronic Kidney Disease|Kidney Disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.