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Variant (rsID / SNP)

rs2277841

FOXRED2

rs2277841 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FOXRED2. Location: chromosome 22, position 36,900,271. The table records no clinical significance for this variant.

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Reference-table entries

FOXRED2Not classified
Variant type
missense_variant
Chromosome / position
22:36900271
HGVS
NM_001102371.2,c.923A>G,p.Asn308Ser
Allele change
Missense_N308S

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.