Variant (rsID / SNP)

rs2241280

rs2241280 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FGF6. Location: chromosome 12, position 4,553,332. The table records no clinical significance for this variant.

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Reference-table entries

FGF6Not classified

Variant type: synonymous_variant
Chromosome / position: 12:4553332
HGVS: NM_020996.3,c.417T>C,p.Val139Val
Allele change: Synonymous_V139V

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.