List of variants in gene APC2 reported as benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_005883.3(APC2):c.2952C>A (p.Thr984=)	rs10413634	0.09185
NM_005883.3(APC2):c.6071C>T (p.Ala2024Val)	rs166453	0.03733
NM_005883.3(APC2):c.2845G>A (p.Ala949Thr)	rs61735597	0.03727
NM_005883.3(APC2):c.4260G>C (p.Gly1420=)	rs148212035	0.00283
NM_005883.3(APC2):c.4470C>T (p.Asp1490=)	rs265272	0.00186

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