Variant (rsID / SNP)
rs2291343
rs2291343 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDH7. Location: chromosome 18, position 63,530,016. The table records no clinical significance for this variant.
Reference-table entries
CDH7Not classified
- Variant type
- missense_variant
- Chromosome / position
- 18:63530016
- HGVS
- NM_001362438.2,c.1727A>G,p.Asn576Ser
- Allele change
- Missense_N576S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.