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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
C1orf122
(P25T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1orf122
(D102N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance