Variant (rsID / SNP)

rs1800822

rs1800822 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FMO3. Location: chromosome 1, position 171,076,935. 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: 1:171076935
Cytoband: 1q24.3
HGVS: NM_001002294.3(FMO3):c.441C>T (p.Ser147=)
Allele change: Synonymous_S84S

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.