Variant (rsID / SNP)
rs10604
rs10604 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to QDPR. Location: chromosome 4, position 17,488,132. Clinical significance in the table: Benign.
Reference-table entries
QDPRBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 4:17488132
- Cytoband
- 4p15.32
- HGVS
- NM_000320.3(QDPR):c.*622T>C
- Allele change
- Silent
Associated conditions / phenotypes
Dihydropteridine reductase deficiency
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.