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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADGRV1
(R437W)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
ADGRV1
(R1841C)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance