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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC17A5
(K136E)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic/Likely pathogenic
SLC17A5
(R39C)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic