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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC110806263, TERT
Single nucleotide variant
Dyskeratosis congenita, autosomal dominant 2
+2 more
GLikely pathogenic
OOncogenic
AR
(E111K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ROS1
(G227S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ROS1
(E2226K +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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