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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HSPG2, LOC126805655
(A2181T +1 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
HSPG2, LOC126805655
(H2162Y +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance