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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LURAP1L-AS1, TYRP1
(K368fs)
Deletion
(frameshift variant)
Oculocutaneous albinism type 3
+2 more
GPathogenic/Likely pathogenic
LURAP1L-AS1, TYRP1
Single nucleotide variant
(splice donor variant)
not provided
+1 more
GPathogenic/Likely pathogenic