Variant (rsID / SNP)

rs2293783

rs2293783 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FOXF2. Location: chromosome 6, position 1,395,043. The table records no clinical significance for this variant.

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Reference-table entries

FOXF2Not classified

Variant type: synonymous_variant
Chromosome / position: 6:1395043
HGVS: NM_001452.2,c.1284T>C,p.Tyr428Tyr
Allele change: Synonymous_Y428Y

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.