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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FOXC1, LOC129995601
(P79Q)
Single nucleotide variant
(missense variant)
not provided
GPathogenic
FOXC1, LOC129995601
(K98del)
Microsatellite
(inframe_deletion)
not provided
GLikely pathogenic