Variant (rsID / SNP)
rs2074504
rs2074504 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRR3. Location: chromosome 6, position 30,530,245. The table records no clinical significance for this variant.
Reference-table entries
PRR3Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:30530245
- HGVS
- NM_025263.4,c.540T>C,p.His180His
- Allele change
- Synonymous_H180H
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.