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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ANKRD26
(T806M +1 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
ANKRD26
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
ANKRD26
(E454D)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ANKRD26
(A174G)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
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