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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MUTYH
Single nucleotide variant
(synonymous variant +1 more)
not provided
+3 more
GBenign/Likely benign
MUTYH
(Y165C +8 more)
Single nucleotide variant
(missense variant +1 more)
MUTYH-related disorder
+4 more
GPathogenic/Likely pathogenic