Variant (rsID / SNP)
rs28614045
rs28614045 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UVSSA. Location: chromosome 4, position 1,374,695. The table records no clinical significance for this variant.
Reference-table entries
UVSSANot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 4:1374695
- HGVS
- NM_001317934.2,c.1780C>A,p.Arg594Arg
- Allele change
- Synonymous_R594R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
