Variant (rsID / SNP)

rs35082957

rs35082957 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PEX10. Location: chromosome 1, position 2,337,992. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

PEX10Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:2337992
Cytoband: 1p36.32
HGVS: NM_002617.4(PEX10):c.843G>A (p.Arg281=)
Allele change: Synonymous_R281R

Associated conditions / phenotypes

Peroxisome biogenesis disorder 6A (Zellweger)|Peroxisome biogenesis disorder, complementation group 7|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.