Variant (rsID / SNP)
rs536455
rs536455 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRG2. Location: chromosome 11, position 57,155,001. The table records no clinical significance for this variant.
Reference-table entries
PRG2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 11:57155001
- HGVS
- NM_001302926.2,c.616C>T,p.His206Tyr
- Allele change
- Missense_H206Y
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.