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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MEIS2
(S116A +2 more)
Single nucleotide variant
(missense variant +1 more)
Cardiac malformation, cleft lip/palate, microcephaly, and digital anomalies
GUncertain significance
MEIS2
Single nucleotide variant
(synonymous variant +1 more)
Cardiac malformation, cleft lip/palate, microcephaly, and digital anomalies
GUncertain significance