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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARNT2, ARNT2-DT
+38 more
Copy number gain
See cases
GUncertain significance
MTHFS, ST20-MTHFS
(S12I)
Single nucleotide variant
(missense variant +2 more)
not specified
+1 more
GUncertain significance
AAGAB, ABHD17C
+278 more
Copy number gain
See cases
GPathogenic
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