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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LMF1
(W464* +3 more)
Single nucleotide variant
(nonsense +2 more)
Lipase deficiency, combined
GPathogenic
LMF1
(V247M +3 more)
Single nucleotide variant
(missense variant +1 more)
Lipase deficiency, combined
+2 more
GUncertain significance
LMF1
(Q130E +3 more)
Single nucleotide variant
(missense variant +1 more)
Lipase deficiency, combined
GUncertain significance
ABCA3, ADCY9
+159 more
Copy number gain
Chromosome 16p13.3 duplication syndrome
GPathogenic
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