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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARHGEF10
Single nucleotide variant
(intron variant)
Autosomal dominant slowed nerve conduction velocity
GLikely benign
ARHGEF10
(D292E +2 more)
Single nucleotide variant
(missense variant)
Autosomal dominant slowed nerve conduction velocity
GUncertain significance