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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PQBP1
(R145fs +1 more)
Microsatellite
(frameshift variant +1 more)
not provided
+4 more
GPathogenic/Likely pathogenic
PQBP1
(P148R +4 more)
Single nucleotide variant
(missense variant)
Renpenning syndrome
GUncertain significance