Variant (rsID / SNP)
rs2280786
rs2280786 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RDM1. Location: chromosome 17, position 34,257,637. The table records no clinical significance for this variant.
Reference-table entries
RDM1Not classified
- Variant type
- missense_variant&splice_region_variant
- Chromosome / position
- 17:34257637
- HGVS
- NM_145654.4,c.95A>G,p.His32Arg
- Allele change
- Silent
Associated conditions / phenotypes
Missense_H32R|Missense_H32R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.