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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARHGEF10
Indel
(splice acceptor variant)
Autosomal dominant slowed nerve conduction velocity
GUncertain significance
ARHGEF10
Deletion
(nonsense)
Autosomal dominant slowed nerve conduction velocity
GUncertain significance