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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MSH6
(R870fs +2 more)
Microsatellite
(frameshift variant)
not provided
+5 more
GPathogenic
MSH6
Duplication
(nonsense)
Lynch syndrome
GPathogenic
FBXO11, MSH6
(D826G +1 more)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities
GPathogenic/Likely pathogenic
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