List of variants in gene APC2 reported as likely benign by Ambry Genetics

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_005883.3(APC2):c.5396C>T (p.Pro1799Leu)	rs73516821	0.00227
NM_005883.3(APC2):c.334G>A (p.Gly112Ser)	rs150959468	0.00185
NM_005883.3(APC2):c.4958G>A (p.Arg1653Gln)	rs555371409	0.00134
NM_005883.3(APC2):c.209C>T (p.Thr70Met)	rs144391493	0.00098
NM_005883.3(APC2):c.3656C>T (p.Ala1219Val)	rs137877386	0.00093
NM_005883.3(APC2):c.1592C>T (p.Ala531Val)
NM_005883.3(APC2):c.1600G>A (p.Val534Met)
NM_005883.3(APC2):c.1628G>A (p.Arg543Gln)
NM_005883.3(APC2):c.322A>C (p.Ser108Arg)
NM_005883.3(APC2):c.323G>T (p.Ser108Ile)
NM_005883.3(APC2):c.4268C>A (p.Ala1423Glu)
NM_005883.3(APC2):c.4412G>A (p.Arg1471Gln)
NM_005883.3(APC2):c.4613C>A (p.Thr1538Lys)
NM_005883.3(APC2):c.4701C>A (p.Ser1567Arg)
NM_005883.3(APC2):c.4873G>A (p.Ala1625Thr)	rs923953881
NM_005883.3(APC2):c.6361T>C (p.Ser2121Pro)
NM_005883.3(APC2):c.6586G>T (p.Val2196Phe)

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