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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MUTYH
Indel
(inframe_indel +1 more)
Familial adenomatous polyposis 2
GPathogenic
MUTYH
(R247G +7 more)
Single nucleotide variant
(missense variant +1 more)
Familial adenomatous polyposis 2
+1 more
GLikely pathogenic
MUTYH
(I223V +7 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+4 more
GUncertain significance
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