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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TYR
(V275F)
Single nucleotide variant
(missense variant)
Oculocutaneous albinism
+4 more
GPathogenic/Likely pathogenic
TYR
(T373K)
Single nucleotide variant
(missense variant)
Oculocutaneous albinism
+5 more
GPathogenic