Variant (rsID / SNP)
rs3026101
rs3026101 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RABEP1. Location: chromosome 17, position 5,280,440. The table records no clinical significance for this variant.
Reference-table entries
RABEP1Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:5280440
- HGVS
- NM_004703.6,c.2055T>C,p.Arg685Arg
- Allele change
- Synonymous_R642R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.