List of variants in gene APC reported as likely benign by Genome Diagnostics Laboratory, Amsterdam University Medical Center

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000038.6(APC):c.3386T>C (p.Leu1129Ser)	rs143638171	0.00250
NM_000038.6(APC):c.705A>G (p.Leu235=)	rs147036141	0.00213
NM_000038.6(APC):c.7514G>A (p.Arg2505Gln)	rs147549623	0.00093
NM_000038.6(APC):c.3173A>G (p.Asp1058Gly)	rs148725540	0.00057
NM_000038.6(APC):c.2322C>T (p.Asp774=)	rs145792879	0.00041
NM_000038.6(APC):c.607C>G (p.Gln203Glu)	rs141576417	0.00033
NM_000038.6(APC):c.6526T>C (p.Leu2176=)	rs183468041	0.00022
NM_000038.6(APC):c.450A>G (p.Lys150=)	rs116020626	0.00013
NM_000038.6(APC):c.6873A>T (p.Gln2291His)	rs148878262	0.00012
NM_000038.6(APC):c.6682A>G (p.Arg2228Gly)	rs199648202	0.00004
NM_000038.6(APC):c.8383G>A (p.Ala2795Thr)	rs369264968	0.00003
NM_000038.6(APC):c.835-3T>C	rs372090940	0.00002
NM_000038.6(APC):c.423-4del	rs730881230
NM_000038.6(APC):c.4704T>C (p.Asp1568=)	rs1554086117

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