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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FAM111B
(Q124fs +1 more)
Insertion
(frameshift variant)
not specified
+1 more
GUncertain significance
FAM111B
(A194G +1 more)
Single nucleotide variant
(missense variant)
Hereditary sclerosing poikiloderma with tendon and pulmonary involvement
GUncertain significance