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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PROKR2
(R268C)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign/Likely benign
PROKR2
(R85H)
Single nucleotide variant
(missense variant)
PROKR2-related condition
+4 more
GConflicting classifications of pathogenicity