Variant (rsID / SNP)
rs10236856
rs10236856 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PEX1. Location: chromosome 7, position 92,135,686. Clinical significance in the table: Benign.
Reference-table entries
PEX1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:92135686
- Cytoband
- 7q21.2
- HGVS
- NM_000466.3(PEX1):c.1804-28G>A
- Allele change
- Silent
Associated conditions / phenotypes
Peroxisome biogenesis disorder 1A (Zellweger)
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.