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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CARD14, SGSH
(R245H)
Single nucleotide variant
(missense variant +1 more)
SGSH-related condition
+4 more
GPathogenic
SGSH
(G122R)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GPathogenic/Likely pathogenic
SGSH
(R74C)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GPathogenic/Likely pathogenic
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