Variant (rsID / SNP)

rs2066743

rs2066743 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PEX1. Location: chromosome 7, position 92,147,374. Clinical significance in the table: Benign.

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Reference-table entries

PEX1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 7:92147374
Cytoband: 7q21.2
HGVS: NM_000466.3(PEX1):c.473-18G>A
Allele change: Silent

Associated conditions / phenotypes

Peroxisome biogenesis disorder 1A (Zellweger)|Zellweger spectrum disorders

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.