Variant (rsID / SNP)

rs2375465

rs2375465 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FOXR2. The table records no clinical significance for this variant.

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Reference-table entries

FOXR2Not classified

Variant type: missense_variant
HGVS: NM_198451.4,c.857T>C,p.Val286Ala
Allele change: Missense_V286A

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.