Variant (rsID / SNP)

rs2266780

rs2266780 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FMO3. Location: chromosome 1, position 171,083,242. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

FMO3Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:171083242
Cytoband: 1q24.3
HGVS: NM_001002294.3(FMO3):c.923A>G (p.Glu308Gly)
Allele change: Missense_E245G

Associated conditions / phenotypes

Trimethylaminuria

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.