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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HPS6, LOC130004578
(M1V)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
HPS6, LOC130004578
(D80fs)
Duplication
(frameshift variant)
Hermansky-Pudlak syndrome
+2 more
GConflicting classifications of pathogenicity
HPS6
(P231R)
Single nucleotide variant
(missense variant)
HPS6-related disorder
+3 more
GUncertain significance
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