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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PYDC1, TRIM72
(A83P)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
TRIM72, PYDC1
(D54G)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance