Variant (rsID / SNP)

rs200676463

rs200676463 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FOXF1. Location: chromosome 16, position 86,545,083. Clinical significance in the table: Benign.

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Reference-table entries

FOXF1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 16:86545083
Cytoband: 16q24.1
HGVS: NM_001451.3(FOXF1):c.908G>A (p.Ser303Asn)
Allele change: Missense_S303N

Associated conditions / phenotypes

Alveolar capillary dysplasia with pulmonary venous misalignment

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.