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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FMO3, LOC126805916
(P153L +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
FMO3, LOC126805916
(V187A +2 more)
Single nucleotide variant
(missense variant)
Trimethylaminuria
GPathogenic
FMO3, LOC126805916
(E308G +2 more)
Single nucleotide variant
(missense variant)
Trimethylaminuria
+1 more
GPathogenic/Likely pathogenic
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