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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GRHPR
(D35fs)
Deletion
(frameshift variant)
not provided
+1 more
GPathogenic
GRHPR
(C57Y)
Single nucleotide variant
(missense variant)
Primary hyperoxaluria, type II
GLikely pathogenic