Variant (rsID / SNP)

rs41311141

rs41311141 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FBXO7. Location: chromosome 22, position 32,880,006. Clinical significance in the table: Benign/Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

FBXO7Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 22:32880006
Cytoband: 22q12.3
HGVS: NM_012179.4(FBXO7):c.540A>G (p.Pro180=)
Allele change: Synonymous_P180P

Associated conditions / phenotypes

Parkinsonian-pyramidal syndrome

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.