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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC52A3
(F457L)
Single nucleotide variant
(missense variant)
Brown-Vialetto-van Laere syndrome 1
+4 more
GUncertain significance
SLC52A3
(P297L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance