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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FAH, LOC112272621
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign/Likely benign
FAH, LOC112272621
(T114M)
Single nucleotide variant
(missense variant)
Tyrosinemia type I
GUncertain significance