Variant (rsID / SNP)

rs61730783

rs61730783 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FBXO7. Location: chromosome 22, position 32,880,067. Clinical significance in the table: Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

FBXO7Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 22:32880067
Cytoband: 22q12.3
HGVS: NM_012179.4(FBXO7):c.601G>A (p.Val201Met)
Allele change: Missense_V201M

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.