Variant (rsID / SNP)
rs35195
rs35195 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDH11. Location: chromosome 16, position 65,025,718. The table records no clinical significance for this variant.
Reference-table entries
CDH11Not classified
- Variant type
- missense_variant
- Chromosome / position
- 16:65025718
- HGVS
- NM_001797.4,c.764C>T,p.Thr255Met
- Allele change
- Missense_T129M
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.