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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATP2B3
(R41Q)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ATP2B3
(L63fs)
Indel
(frameshift variant)
not provided
GUncertain significance
ATP2B3
(I590F +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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