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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GDAP1
Deletion
(intron variant)
GDAP1-related disorder
+7 more
GConflicting classifications of pathogenicity
GDAP1
Single nucleotide variant
(splice acceptor variant +1 more)
Charcot-Marie-Tooth disease type 4A
+2 more
GPathogenic/Likely pathogenic
GDAP1
Single nucleotide variant
(synonymous variant +1 more)
Charcot-Marie-Tooth disease
+4 more
GLikely benign
GDAP1
(R282H +3 more)
Single nucleotide variant
(missense variant +1 more)
Charcot-Marie-Tooth disease type 4A
+2 more
GPathogenic
GDAP1
(Q263E)
Single nucleotide variant
(missense variant)
GDAP1-related disorder
GUncertain significance
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