Variant (rsID / SNP)
rs236843
rs236843 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PARD3B. Location: chromosome 2, position 205,829,991. The table records no clinical significance for this variant.
Reference-table entries
PARD3BNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 2:205829991
- HGVS
- NM_001302769.2,c.339C>T,p.Ala113Ala
- Allele change
- Synonymous_A113A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.