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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MTR
(A129P)
Single nucleotide variant
(missense variant +1 more)
Homocystinuria
+1 more
GLikely pathogenic
MTR
(P1173L +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+3 more
GPathogenic