C1851124[trait identifier] AND "GenomeConnect, ClinGen"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 41509	NM_000038.6(APC):c.607C>G (p.Gln203Glu)	APC (Q203E +3 more)	Single nucleotide variant (missense variant +1 more)	not provided +5 more	GConflicting classifications of pathogenicity
Select item 184937	NM_000038.6(APC):c.994C>T (p.Arg332Ter)	APC (R314* +6 more)	Single nucleotide variant (nonsense +1 more)	not provided +8 more	GPathogenic
Select item 127281	NM_000038.6(APC):c.2413C>T (p.Arg805Ter)	APC (R805* +12 more)	Single nucleotide variant (nonsense)	Familial multiple polyposis syndrome +6 more	GPathogenic

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