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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FMO3
(V58I +1 more)
Single nucleotide variant
(missense variant +1 more)
Trimethylaminuria
+2 more
GConflicting classifications of pathogenicity
FMO3, LOC126805916
(V123E +2 more)
Single nucleotide variant
(missense variant)
Trimethylaminuria
GUncertain significance
FMO3, LOC126805916
(P153L +2 more)
Single nucleotide variant
(missense variant)
Trimethylaminuria
+1 more
GConflicting classifications of pathogenicity
FMO3, LOC126805916
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign/Likely benign
FMO3
(E299Q +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
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