Variant (rsID / SNP)
rs77235035
rs77235035 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PEAR1. Location: chromosome 1, position 156,877,797. The table records no clinical significance for this variant.
Reference-table entries
PEAR1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 1:156877797
- HGVS
- NM_001080471.3,c.856C>A,p.Arg286Arg
- Allele change
- Synonymous_R222R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
