Variant (rsID / SNP)

rs894469

rs894469 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FMO5. Location: chromosome 1, position 146,672,906. The table records no clinical significance for this variant.

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Reference-table entries

FMO5Not classified

Variant type: synonymous_variant
Chromosome / position: 1:146672906
HGVS: NM_001461.4,c.1011G>A,p.Pro337Pro
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.