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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC9A6
(I137N +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
SLC9A6
(I242T +3 more)
Single nucleotide variant
(missense variant)
Christianson syndrome
GUncertain significance