Variant (rsID / SNP)

rs141133579

rs141133579 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PEX19. Location: chromosome 1, position 160,249,857. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

PEX19Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:160249857
Cytoband: 1q23.2
HGVS: NM_002857.4(PEX19):c.771+3A>G
Allele change: Silent

Associated conditions / phenotypes

Peroxisome biogenesis disorder 12A (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.