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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TINF2
(R282H +1 more)
Single nucleotide variant
(missense variant)
Dyskeratosis congenita, autosomal dominant 3
+4 more
GPathogenic
TINF2
(L135F +1 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GUncertain significance
TINF2
(P88T)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
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