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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AAAS
(Q389fs +1 more)
Deletion
(frameshift variant)
Glucocorticoid deficiency with achalasia
GPathogenic
AAAS
(I184V +1 more)
Single nucleotide variant
(missense variant)
Glucocorticoid deficiency with achalasia
GUncertain significance
AAAS
(Q15K)
Single nucleotide variant
(missense variant)
Glucocorticoid deficiency with achalasia
+1 more
GPathogenic
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