C3272841[trait identifier] AND "Division of Medical Genetics, Universi - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 41766	NM_001048174.2(MUTYH):c.850-2A>G	MUTYH	Single nucleotide variant (splice acceptor variant)	MUTYH-related disorder +5 more	GConflicting classifications of pathogenicity
Select item 142805	NM_001048174.2(MUTYH):c.420+2T>C	MUTYH	Single nucleotide variant (splice donor variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GPathogenic/Likely pathogenic
Select item 234229	NM_001048174.2(MUTYH):c.305-1G>C	MUTYH	Single nucleotide variant (splice acceptor variant +1 more)	not provided +4 more	GPathogenic

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ClinVar