"Center of Medical Genetics and Primary Health Care"[submitter] AND "A - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 127944	NM_004655.4(AXIN2):c.2285G>A (p.Ser762Asn)	AXIN2 (S762N +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 415218	NM_004655.4(AXIN2):c.2083G>T (p.Ala695Ser)	AXIN2 (A695S +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity