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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
C2
(H269P +4 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
C2
(K364fs +4 more)
Microsatellite
(frameshift variant)
not provided
GLikely pathogenic