Variant (rsID / SNP)

rs3804545

rs3804545 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PEX3. Location: chromosome 6, position 143,811,258. Clinical significance in the table: Likely benign.

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Reference-table entries

PEX3Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 6:143811258
Cytoband: 6q24.2
HGVS: NM_003630.3(PEX3):c.*895G>A
Allele change: Silent

Associated conditions / phenotypes

Peroxisome biogenesis disorder 10A (Zellweger)

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.