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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PROZ
(P112A +1 more)
Single nucleotide variant
(missense variant)
PROZ-related disorder
GLikely benign
PCID2, PROZ
Single nucleotide variant
(synonymous variant)
PROZ-related disorder
GLikely benign
PCID2, PROZ
(L291F +1 more)
Single nucleotide variant
(missense variant)
PROZ-related disorder
+1 more
GBenign
PCID2, PROZ
(R295H +1 more)
Single nucleotide variant
(missense variant)
PROZ-related disorder
GLikely benign
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