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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KLF7
(S107L +2 more)
Single nucleotide variant
(missense variant)
KLF7-related neurodevelopmental disorder
GUncertain significance
KLF7
(T104M +2 more)
Single nucleotide variant
(missense variant)
Delayed gross motor development
+7 more
GConflicting classifications of pathogenicity