Variant (rsID / SNP)

rs56404456

rs56404456 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FOXF1. Location: chromosome 16, position 86,547,001. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

FOXF1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 16:86547001
Cytoband: 16q24.1
HGVS: NM_001451.3(FOXF1):c.*310C>T
Allele change: Silent

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.