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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARHGEF10
(T182A +2 more)
Single nucleotide variant
(missense variant)
Autosomal dominant slowed nerve conduction velocity
GUncertain significance
ARHGEF10
(N844K +2 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance