Variant (rsID / SNP)
rs35418374
rs35418374 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRF1. Location: chromosome 10, position 72,360,648. Clinical significance in the table: Benign/Likely benign.
Reference-table entries
PRF1Benign
- Clinical significance (as recorded)
- Benign/Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 10:72360648
- Cytoband
- 10q22.1
- HGVS
- NM_001083116.3(PRF1):c.11G>A (p.Arg4His)
- Allele change
- Missense_R4H
Associated conditions / phenotypes
Aplastic anemia|Familial hemophagocytic lymphohistiocytosis 2|Autoinflammatory syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.