Variant (rsID / SNP)
rs12960862
rs12960862 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CNDP1. Location: chromosome 18, position 72,234,635. The table records no clinical significance for this variant.
Reference-table entries
CNDP1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 18:72234635
- HGVS
- NM_032649.6,c.723C>T,p.Tyr241Tyr
- Allele change
- Synonymous_Y241Y
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.