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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MSH6
(E16fs +2 more)
Deletion
(frameshift variant)
not provided
GPathogenic
MSH6
(F1021fs +2 more)
Duplication
(frameshift variant)
Hereditary nonpolyposis colorectal neoplasms
+3 more
GPathogenic/Likely pathogenic