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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC122056894, NFIA
Single nucleotide variant
(intron variant)
Chromosome 1p32-p31 deletion syndrome
GUncertain significance
NFIA
(W75* +2 more)
Single nucleotide variant
(nonsense)
Chromosome 1p32-p31 deletion syndrome
GPathogenic