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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HSPG2
(A1335T +1 more)
Single nucleotide variant
(missense variant)
HSPG2-realted disorder
GUncertain significance
HSPG2
(R1060W +1 more)
Single nucleotide variant
(missense variant)
HSPG2-realted disorder
GUncertain significance