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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
C10orf55, LOC126860960
+1 more
(E166G +2 more)
Single nucleotide variant
(missense variant)
Quebec platelet disorder
GUncertain significance
C10orf55, LOC126860960
+1 more
(M166L +2 more)
Single nucleotide variant
(missense variant)
Quebec platelet disorder
+1 more
GUncertain significance