Variant (rsID / SNP)

rs114291166

rs114291166 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FMN2. Location: chromosome 1, position 240,370,702. The table records no clinical significance for this variant.

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Reference-table entries

FMN2Not classified

Variant type: missense_variant
Chromosome / position: 1:240370702
HGVS: NM_001305424.2,c.2602A>G,p.Thr868Ala
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.