Variant (rsID / SNP)

rs2266782

rs2266782 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FMO3. Location: chromosome 1, position 171,076,966. Clinical significance in the table: Benign.

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Reference-table entries

FMO3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:171076966
Cytoband: 1q24.3
HGVS: NM_001002294.3(FMO3):c.472G>A (p.Glu158Lys)
Allele change: Missense_E95K

Associated conditions / phenotypes

Trimethylaminuria|See cases

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.