List of variants in gene combination MUTYH, TOE1 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001128425.2(MUTYH):c.12C>A (p.Leu4=)	rs876659717
NM_001128425.2(MUTYH):c.12C>T (p.Leu4=)	rs876659717
NM_001128425.2(MUTYH):c.22C>T (p.Leu8=)	rs753502884
NM_001128425.2(MUTYH):c.24G>C (p.Leu8=)	rs1570591790
NM_001128425.2(MUTYH):c.28C>A (p.Arg10Ser)	rs1570591700
NM_001128425.2(MUTYH):c.31C>T (p.Leu11=)	rs878854188
NM_001128425.2(MUTYH):c.33G>A (p.Leu11=)
NM_001128425.2(MUTYH):c.9G>A (p.Pro3=)	rs958040221
NM_001128425.2(MUTYH):c.9G>C (p.Pro3=)	rs958040221
NM_001128425.2(MUTYH):c.9G>T (p.Pro3=)	rs958040221

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