Variant (rsID / SNP)
rs782633
rs782633 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PNPT1. Location: chromosome 2, position 55,898,203. Clinical significance in the table: Benign.
Reference-table entries
PNPT1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:55898203
- Cytoband
- 2p16.1
- HGVS
- NM_033109.5(PNPT1):c.976+251T>C
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.