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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GNPTAB
(C505Y)
Single nucleotide variant
(missense variant)
Pseudo-Hurler polydystrophy
+3 more
GPathogenic/Likely pathogenic
GNPTAB
(V78del)
Microsatellite
(inframe_deletion)
not specified
+1 more
GUncertain significance