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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HSPG2
(R3693W +1 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
HSPG2
(R413Q)
Single nucleotide variant
(missense variant)
not provided
+3 more
GBenign/Likely benign