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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TYR
(R77Q)
Single nucleotide variant
(missense variant)
TYR-related disorder
+5 more
GPathogenic
TYR
(P406L)
Single nucleotide variant
(missense variant)
Oculocutaneous albinism
+8 more
GPathogenic/Likely pathogenic