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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126805916, FMO3
Single nucleotide variant
(missense variant)
Trimethylaminuria
+3 more
GBenign
FMO3, LOC126805916
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign
FMO3, LOC126805916
Single nucleotide variant
(intron variant)
Trimethylaminuria
+2 more
GBenign
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