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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PSAT1
(A99V)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic/Likely pathogenic
PSAT1
(H335L)
Single nucleotide variant
(missense variant +1 more)
Neu-Laxova syndrome 2
GUncertain significance