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Links from Gene

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FOXK2, LOC130062047
(A132V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FOXK2, LOC130062047
Single nucleotide variant
(intron variant)
not provided
GLikely benign