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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MFSD8
(P412L +8 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GPathogenic/Likely pathogenic
MFSD8
(E381* +8 more)
Single nucleotide variant
(nonsense)
Neuronal ceroid lipofuscinosis 7
+3 more
GPathogenic