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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARHGEF10
(E65* +1 more)
Single nucleotide variant
(nonsense)
Autosomal dominant slowed nerve conduction velocity
GUncertain significance
ARHGEF10
(E410G +2 more)
Single nucleotide variant
(missense variant)
Autosomal dominant slowed nerve conduction velocity
GUncertain significance
ARHGEF10
(S688N +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
ARHGEF10
(A712S +2 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GConflicting classifications of pathogenicity
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