Variant (rsID / SNP)

rs2020865

rs2020865 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FMO2. Location: chromosome 1, position 171,176,912. The table records no clinical significance for this variant.

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Reference-table entries

FMO2Not classified

Variant type: missense_variant
Chromosome / position: 1:171176912
HGVS: NM_001460.5,c.1239T>G,p.Asn413Lys
Allele change: Missense_N193K

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.