Variant (rsID / SNP)

rs4645855

rs4645855 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FOS. Location: chromosome 14, position 75,746,869. The table records no clinical significance for this variant.

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Reference-table entries

FOSNot classified

Variant type: intron_variant
Chromosome / position: 14:75746869
HGVS: NM_005252.4,c.393+38G>A
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.