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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ERBB4
(G1256R +1 more)
Single nucleotide variant
(missense variant)
Amyotrophic lateral sclerosis
GLikely pathogenic
ERBB4
(M1059T)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
ERBB4
(H374Q)
Single nucleotide variant
(missense variant)
Amyotrophic lateral sclerosis
+3 more
GConflicting classifications of pathogenicity
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